# medications

human_id: huC3160A
name: Chloroquine Phosphate
dosage: 500 MG
start_date: 2008-11-05 (refill)
frequency:
  FOR MALARIA PROPHYLAXIS-ONE TABLET   ONCE WEEKLY WITH PLENTY OF LIQUID ON A FULL STOMACH. BEGIN 2 WEEKS BEFORE DEPARTURE. TAKE ONCE WEEKLY DURING   TRIP ON THE SAME DAY OF THE WEEK AND CONTINUE FOR 4 MORE WEEKS AFTER      RETURN


human_id: hu925B56
name: *NYST/HCO/Q-DRYL
dosage: 100,000 unit/mL
start_date: 2011-08-22 (refill)
frequency:
  SHAKE LIQUID WELL AND SWISH AND SPIT 2 TEASPOONSFUL BY MOUTH EVERY 3 TO 4 HOURS AS NEEDED FOR MOUTH SORES


human_id: hu925B56
name: DEXAMETHASONE 4MG TABLETS
dosage: 4 mg
start_date: 2011-09-20 (refill)
frequency:
  TAKE 2 TABLETS BY MOUTH AT 10 PM THE NIGHT BEFORE TREATMENT AND 1 TABLET AT 8 AM THE MORNING OF THE TREATMENT


human_id: hu925B56
name: ONDANSETRON 8MG TABLETS
dosage: 8 mg
start_date: 2011-06-27 (refill)
frequency:
  TAKE 1 TABLET BY MOUTH TWICE DAILY ON DAY 1 , 2 , AND 3 OF CHEMO, THEN EVERY 6 HOURS AS NEEDED FOR NAUSEA THEREAFTER


human_id: huA545A9
name: MALARONE 250/100 TABLETS
dosage: 250-100 mg Tablet
start_date: 2010-10-08 (refill)
frequency:
  TAKE 1 TABLET BY MOUTH DAILY . BEGIN 1-2 DAYS BEFORE ENTERING MALARIOUS AREA, TAKE DAILY WHILE THERE AND FOR 7 DAYS AFTER LEAVING. WITH FOOD OR MILK


human_id: hu1C2BAE
name:
  Flulaval Quad 2014-2015 60 mcg (15 mcg x 4)/0.5 mL IM suspension INJECT 0.5 ML INTRAMUSCULARLY AS DIRECTED


human_id: hu3B8141
name: WARFARIN SOD 5MG TABLETS(PEACH)
dosage: 5 mg Tablet
start_date: 2011-05-08 (refill)
frequency:
  TAKE ONE TABLET BY MOUTH EVERY DAY ALONG WITH TWO OF THE 1 MG TABLETS FOR A TOTAL DAILY DOSE OF 7 MG


human_id: huF2EC1A
name: CLOMIPRAMINE 25MG CAPSULES
dosage: 25 mg Capsule
start_date: 2010-04-22 (refill)
frequency:
  TAKE 2 CAPSULES BY MOUTH EVERY NIGHT AT BEDTIME FOR 2 DAYS , THEN TAKE 3 CAPSULES BY MOUTH EVERY NIGHT AT BEDTIME


human_id: hu957276
name:
  Crestor 10 mg 1x/day, Zetia 10 mg 1x/day, Avapro 300 mg 1x/day, Plavix 75 mg 1x/day, Aspirin 325 mg 1x/day, Ambien 10 mg at bedtime, Spiriva Handihaler 18 mcg 1x/day, Pulmicort and Brovana nebulizer 2x/day, Flomax 0.4 mg 1x/day, Lasix 40 mg... [truncated]


human_id: huBD8A03
name: GABAPENTIN 300 MG CAPSULE
dosage: 300
start_date: 2012-01-10 (refill)
frequency:
  Take 7, TAKE 2 CAPSULES BY MOUTH EVERY MORNING , TAKE 2 CAPSULES MIDDAY AND TAKE 3 CAPSULES AT BEDTIME


human_id: hu748373
dosage: various
frequency: Take 1, 1 time per day
name:
  unabme to afford medication at this time. lisinopril, methotrexate, levothyroxine, folic acid, ferrous sulfate, clobex lotion, topamax, buspar, concerta.


human_id: huDD1522
name: LISINOPRIL 20 MG TABLET
dosage: 20
start_date: 2014-05-23 (refill)
frequency:
  TAKE 1/2 TABLET DAILY FOR 1 WEEK AND CHECK BLOOD PRESSURE IF REMAINS ABOVE 140/90 TAKE A FULL TABLET


human_id: hu7FC773
frequency: Take 1, 1
name:
  Calcium 600 with Vitamin D3 600 mg (1,500 mg)-400 unit capsule Take 1 capsule(s) every day by oral route for 30 days.


human_id: hu7FC773
name:
  Spiriva with HandiHaler 18 mcg &amp; inhalation capsules INHALE ONE CAPSULE VIA HANDIHALER BY MOUTH EVERY DAY


human_id: hu7FC773
start_date: 2015-01-08
name:
  Symbicort 160 mcg-4.5 mcg/actuation HFA aerosol inhaler 2 PUFF(S), 80 MCG-4.5 MCG/INH, 2 TIMES A DAY


# immunizations

human_id: hu957276
date: 2004-01-01
name:
  Have all regular immunizations (measles/mumps/rubella and small pox), plus yearly flu vacinations and the pnuemonis vacination.


# specimens

human_id: hu43860C
href: https://my.pgp-hms.org/collection_events/1
text: PGP Blood Collection
log_date: 2011-09-15 17:09:29 UTC
log_text: Coriell Institute for Medical Research
log_description: Sample received by researcher
description:
  Sample 62561302 (whole blood) received 2011-09-15 17:09:46 UTC by Coriell Institute for Medical Research.


human_id: hu6E4515
href: https://my.pgp-hms.org/collection_events/5
text: PGP Tissues
log_date: 2011-11-08 19:24:03 UTC
log_text: Harvard University
log_description: Sample received by researcher
description:
  Sample 93757805 (liver biopsy (normal tissue)) received 2011-11-08 19:23:19 UTC by Harvard University.


human_id: huA90CE6
href: https://my.pgp-hms.org/collection_events/1
text: PGP Blood Collection
log_date: 2011-09-15 12:04:44 UTC
log_text: Coriell Institute for Medical Research
log_description: Sample received by researcher
description:
  Sample 76694502 (whole blood) received 2011-09-15 12:04:53 UTC by Coriell Institute for Medical Research.


# allergies

human_id: hu94331C
severity: MILD
name:
  Penicillins, erythromycin, sulfas, cats, dogs, horses, other animals with fur, molds, pollens, birch tree, etc.


human_id: hu433D3A
severity: Severe
name:
  possible cough with enalapril---did not take enalapril, but may have been near some in a lab when I experienced a hard to control cough--- and my mother coughed when given enalapril.


# test_results

human_id: hu7123C1
name: Comprehensive Metabolic Panel
date: 2014-05-01
result:
  Na 142, K 4.7, Cl 102, CO2 30, BUN 14, Cr 1.0,  eGFR &gt;60, Glc 109*, Ca 10.5*, TP 7.3, Alb 4.7, TB 1.3*, AP 51, AST 32, ALT 31, AG 10, BUN/Cr 14, AST/ALT 1.0


human_id: hu7123C1
name: Comprehensive Metabolic Panel
date: 2013-12-05
result:
  Na 140, K 4.6, Cl 102, CO2 28, Glc 106*, BUN 21, Cr 1.1, Ca 9.8, TP 7.0, Alb 4.4, TB 0.4, AP 40, AST 29, ALT 29, AG 10, S/CR 19, A/AR 1.0, eGFR &gt;60


human_id: hu7123C1
name: Comprehensive Metabolic Panel
date: 2013-01-17
result:
  Na 141, K 4.6, Cl 100, CO2 30, Glc 113*, BUN 18, Cr 1.0, Ca 9.8, TP 7.1, Alb 4.5, TB 0.5, AP 41, AST 19, ALT 16, AG 11, S/CR 18, A/AR 1.2, eGFR &gt;60


human_id: hu7123C1
name: Comprehensive Metabolic Panel
date: 2012-12-27
result:
  Na 144, K 4.5, Cl 100, CO2 30, Glc 105*, BUN 13, Cr 1.1, Ca 10.8*, TP 7.5, Alb 5.1, TB 1.5, AP 45, AST 24, ALT 14, AG 14, S/CR 12, A/AR 1.7, eGFR &gt;60


human_id: hu7123C1
name: Comprehensive Metabolic Panel
date: 2010-11-18
result:
  Na 141, K 4.6, Cl 103, BUN 16, CO2 28, Glc 101, Cr 0.9, Ca 10.0, TP 7.4, Alb 4.6, TB 1.2, ALT 18, AST 31, AP 43, AG 10, S/CR 18, A/AR 1.7, eGFR &gt;60


human_id: hu7123C1
name: Comprehensive Metabolic Panel
date: 2010-05-13
result:
  Na 142, K 4.4, Cl 103, BUN 11, CO2 28, Glc 107, Cr 1.0, Ca 09.9, TP 7.2, Alb 4.4, TB 1.2, ALT 16, AST 23, AP 41, AG 15, S/CR 11, A/AR 1.4, eGFR &gt;60


human_id: hu7123C1
name: Comprehensive Metabolic Panel
date: 2009-11-19
result:
  Na 135, K 4.1, Cl 098, BUN 15, CO2 26, Glc 105, Cr 1.0, Ca 09.9, TP 7.6, Alb 4.7, TB 1.4, ALT 18, AST 27, AP 39, AG 15, S/CR 15, A/AR 1.5, eGFR &gt;60


human_id: hu7123C1
name: Comprehensive Metabolic Panel
date: 2009-07-09
result:
  Na 141, K 4.2, Cl 102, BUN 15, CO2 27, Glc 110, Cr 1.0, Ca 10.2, TP 7.4, Alb 4.6, TB 1.0, ALT 19, AST 23, AP 44, AG 16, S/CR 15, A/AR 1.2, eGFR &gt;60


human_id: hu7123C1
name: Comprehensive Metabolic Panel
date: 2008-09-04
result:
  Na 141, K 4.4, Cl 103, BUN 15, CO2 27, Glc 104, Cr 0.9, Ca 10.3, TP 7.2, Alb 4.2, TB 0.9, ALT 18, AST 21  AP 46, AG 15, S/CR 17, A/AR 1.2, eGFR &gt;60


human_id: hu7123C1
name: Comprehensive Metabolic Panel
date: 2007-06-15
result:
  Na 135, K 3.9, Cl 095, BUN 16, CO2 27, Glc 087, Cr 1.1, Ca 10.2, TP 7.7, Alb 4.6, TB 1.1, ALT 15, AST 23, AP 46, AG 17, S/CR 15, A/AR 1.5, eGFR &gt;60


human_id: hu7123C1
name: Comprehensive Metabolic Panel
date: 2006-11-13
result:
  Na 139, K 3.9, Cl 101, BUN 14, CO2 26, Glc 099, Cr 1.1, Ca 10.1, TP 7.6, Alb 4.4, TB 0.8, ALT 13, AST 23, AP 43, AG 16, S/CR 13, A/AR 1.8, eGFR &gt;60


human_id: hu7123C1
name: Urinalysis
date: 2006-08-25
result:
  SG 1.026, APP Clear, COL Yellow, GLC Neg, BIL Neg, KET Trace, BLD Neg, pH 6.0, PRO Neg, LE Neg, NIT Neg, MUC Occ, RBC 1-8, WBC 1-5, BAC Rare


human_id: hu7123C1
name: Comprehensive Metabolic Panel
date: 2006-08-25
result:
  Na 143, K 4.0, Cl 105, BUN 13, CO2 30, Glc 092, Cr 1.0, Ca 09.9, TP 7.6, Alb 4.3, TB 0.5, ALT 12, AST 21, AP 46, AG 12, S/CR 13, A/AR 1.8, eGFR &gt;60


human_id: hu7123C1
name: Urinalysis
date: 2004-10-14
result:
  SG 1.008, APP Clear, COL Yellow, GLC Neg, BIL Neg, KET Neg, BLD Neg, pH 7.0, PRO Neg, LE Neg, NIT Neg, MUC None, RBC None, WBC None, BAC None


human_id: hu7123C1
name: Comprehensive Metabolic Panel
date: 2004-10-14
result:
  Na 138, K 4.3, Cl 101, CO2 31, Glc 90, BUN 16, Cr 0.9, Ca 10.0, TP 7.7, Alb 4.5, TB 1.0, AP 51, AST 18, ALT 16, AG 10, S/CR 18


human_id: hu925B56
name: H1N1 Vaccination Indications
date: 2009-12-16
result:
  Age 25 to 64 years with health condition associated with higher risk for influenza-related complications


human_id: hu329CC4
name: TRANSCRIPTIONS
date: 2013-09-26
result:
  DIAGNOSISÂ Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â  SKIN, LEFT GREAT TOENAIL, (NAIL CLIPPING)Â Â Â Â Â Â Â Â ONYCHOMYCOSISCLINICAL INFORMATIONÂ Â Â Â Â Â Â Â Â Â  Â Â Â Â Â Â Â Â  Suspected Diagnosis: R/O ONYCHOMYCOSIS.Â Â Â Â Â Â Â Â Clinical Information: UnlistedÂ Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Collected by: ASWÂ Â Â Â Â Â Oth


human_id: hu329CC4
name: NAR
date: 2011-04-12
result:
  EXAM: MR C-SPINE WITHOUT CONTRASTEXAM DATE:Â Â 4/12/2011COMPARISON: None.INDICATION:  Chronic neck pain with bilateral radicular symptoms.TECHNIQUE: Sagittal T1, sagittal T2, sagittal STIR axial T1 and axial T2-weighted sequences of the cervical spine.FINDI


human_id: hu329CC4
name: NAR
date: 2011-02-10
result:
  EXAM: FOOT 3+ VIEWS, RIGHTTECHNIQUE: AP, lateral, oblique, sesamoid viewEXAM DATE: 2/10/2011 COMPARISON: NoneINDICATION: Signs/Symptoms: DeformityÂ Â Suspected dx: ArthritisÂ Â Duration: 2 wks to 6 monthsÂ Â Comments:Please take weight bearing views. Please tak


human_id: hu329CC4
name: NAR
date: 2002-07-23
result:
  LT KNEE PAIN, COMMENT: 03325LEFT KNEE:CLINICAL HISTORY:Pain.FINDINGS:AP, lateral and patellar views demonstrate mild medialcompartmental narrowing and spurring.Â Â The patellofemoral joint isnormal.Â Â There is no evidence of a joint effusion. IMPRESSION:MILD


human_id: hu2D21C5
name: Stool Culture
date: 2015-01-26
result:
  Culture negative for enteric pathogens: Salmonella, Shigella, Campylobacter, Yersinia, Aeromonas, Plesiomonas, E. coli 0157,Vibrio(Jun-Sep)


human_id: hu2D21C5
name: Ova And Parasites
date: 2015-01-26
result:
  No helminth eggs, larvae or adult forms by formalin concentration.No protozoan cysts or trophozoites by trichrome stain (PVA).


human_id: hu2D21C5
name: Surgical Pathology R
date: 2015-01-26
result:
  Â Â Â Â  JOHNS HOPKINSÂ Â Â Â Patient: KELLY,WILLIAMÂ Â Â Â Â Â Â Â Â Â Path# S15-5341Â Â Â Â Â Â  REFERENCEÂ Â Â Â Â Â LABORATORIESÂ Â Â Â JHH MR # 3-473-23-97Â Â Â Â Â Â Accessioned 01/26/2015Â Â  Surgical Pathology Birthdate: 08/28/1986Â Â (Age 28) Loc: WMSURÂ Â Â Â Consult ServiceÂ Â Â Â 401 N. Broadwa


human_id: hu2D21C5
name: NAR
date: 2011-03-28
result:
  Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â JOHNS HOPKINS BAYVIEW MEDICAL CENTERÂ Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â IMAGING DEPARTMENTNAME:Â Â Â Â Â Â Â Â  KELLY, WILLIAMPatient name: KELLY,WILLIAMÂ Â  Unit #:BV01656339Â Â DOB: 08/28/1986Â Â Â Â Â Â Account #:MC623807435Â Â Date of Exam:03/26/11Â Â Â Â 032


human_id: huE5A9A3
name: IMP
date: 2014-08-12
result:
  Stable postoperative changes from resection of a known intradural paraganglioma at the L4 level with no evidence of recurrent mass.


human_id: huE5A9A3
name: NAR
date: 2013-10-07
result:
  West Virginia Univ. Hospital1 Medical Center Dr.Morgantown, WVÂ Â ENDOSCOPY PROCEDURE REPORTPATIENT:Â Â Cockburn, AndrewÂ Â MR#:Â Â 007311566 BIRTHDATE:Â Â 02/08/1953Â Â GENDER:Â Â maleENDOSCOPIST:Â Â Gorman J. Reynolds, MDÂ Â ASSISTANT:Â Â Meredith Waters, RNREFERRING PHYSI


human_id: huE5A9A3
name: IMP
date: 2013-09-16
result:
  Degenerative changes are identified in the acromioclavicular joint.Â Â The glenohumeral joint space remains preserved.Â Â There is no abnormal high riding of the humeral head.Â Â No acute bony injury is seen.


human_id: huE5A9A3
name: IMP
date: 2013-08-13
result:
  Stable postoperative changes of an intradural paraganglioma resection from the L4 level are identified without any recurrent tumor.


human_id: huE5A9A3
name: IMP
date: 2012-09-28
result:
  There is no evidence for acute bony abnormality.Â Â There is mild lateral tilt of the patella.Â Â Bony alignment is otherwise preserved.


human_id: huE5A9A3
name: NAR
date: 2012-05-21
result:
  Clinical History: This is a 59-year-old man without known coronary disease who presents with atypical angina. Based on age, sex, symptoms, and risk factors, the pretest probability of coronary disease is intermediate. Based upon his exercise test performa


human_id: huE5A9A3
name: NAR
date: 2012-05-21
result:
  Protocol BRUCETime In Exercise Phase 763 SMax Heart Rate 164 BPMMax Predicted Heart Rate 161 BPMMax. Systolic BP 184 mmHgMax Diastolic BP 76 mmHgMax Work Load 147Exercise Stress Study: NegativeECG:Â Â  NegativeSymptom:Â Â  NegativeChronotropic Response:Â Â  Nor


human_id: huE5A9A3
name: NAR
date: 2012-05-11
result:
  Patient: Andrew F Cockburn MRN: 007311566Â Â Â Â Â Â Â Â Â Â Â Â Procedure:Â Â XR AP MOBILE CHEST History:Â Â  The heart and vessels are unremarkable.Â Â The lungs are clear.Â Â The costophrenic angles are sharp.Â Â No abnormalities are seen on limited evaluation of the bones.


human_id: huE5A9A3
name: NAR
date: 2012-05-11
result:
  Ventricular Rate 57 BPMAtrial Rate 57 BPMP-R Interval 162 msQRS Duration 98 msQT 428 msQTc 416 msP Axis 30 degreesR Axis -20 degreesT Axis 33 degreesSinus bradycardiaOtherwise normal ECGConfirmed by SIKORA MD, ROSANNA (528), editor REED, STEPHANIE (303) o


human_id: huE5A9A3
name: Rheumatoid Factor
date: 2011-07-27
result:
  &lt;10Reference range: 0 to 15Unit: IU/mL(NOTE)Test performed at Warde Medical Laboratory,Ann Arbor, MI 48108


human_id: huE5A9A3
name: PROTEIN S %
date: 2010-04-16
result:
  37Reference range: 50 to 140Unit: %(NOTE)Test performed at Warde Medical Laboratory,Ann Arbor, MI 48108


human_id: huE5A9A3
name: PROTEIN C (ACTIVITY)
date: 2010-04-16
result:
  93Reference range: 70 to 130Unit: %(NOTE)Heparin levels up to 1 IU/ML do not affecttest results.Â Â Higher levels may causeelevated Protein C levels.Test performed at Warde Medical Laboratory,Ann Arbor, MI 48108


human_id: huE5A9A3
name: PROTEIN C AG
date: 2010-04-16
result:
  87Reference range: 72 to 160Unit: %(NOTE)Test performed at Warde Medical Laboratory,Ann Arbor, MI 48108


human_id: huE5A9A3
name: CARDIOLIPIN AB IGA
date: 2010-04-16
result:
  1.2Unit: APL(NOTE)Cardiolipin Antibody, IgA&lt;12Â Â  APL: Absent or none detected12-19 APL: Inconclusive20-80 APL: Moderate positive&gt;80Â Â  APL: High positiveTest performed at Warde Medical Laboratory,Ann Arbor, MI 48108


human_id: huE5A9A3
name: LIPOPROTEIN (a)
date: 2010-04-16
result:
  5Reference range: 0 to 30Unit: mg/dL(NOTE)Levels greater than 30 mg/dL correlatewith an increased risk for coronary heartdisease.Â Â Utermann,G., Et Al, Proc. Natl.Acad. Sci. USA 86:4171-4174 (1989).Test performed at Warde Medical Laboratory,Ann Arbor, MI 4


human_id: hu97DA8A
name: NAR
date: 2016-09-01
result:
  FINAL DIAGNOSISA) Colon, ascending, 2-5 mm polyps x 4 (polypectomy):- Tubular adenoma(s), no high-grade dysplasia.- Hyperplastic polyp(s).B) Colon, descending and sigmoid, 4-5 mm polyps x 4 (polypectomy):- Tubular adenoma, no high-grade dysplasia.- Hyperp


human_id: hu97DA8A
name: NAR
date: 2016-09-01
result:
  University of Colorado (UCO001)____________________________________________________________________________Patient Name: Lawrence HunterÂ Â Â Â Â Â Â Â MRN: 1557542Date of Birth: 1/18/1961Â Â Â Â Â Â Â Â Â Â Â Â  Admit Type: OutpatientAge: 55Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Roo


human_id: hu97DA8A
name: NAR
date: 2012-12-04
result:
  FINAL DIAGNOSISA) Colon, ascending, transverse, 2 x 3-5mm polyps, biopsy:-Â Â  Tubular adenoma; negative for high grade dysplasia-Â Â  Separate fragment of unremarkable colonic mucosaB) Colon, descending, sigmoid, 4 x 2-7mm polyps, biopsies:-Â Â Fragments of tu


human_id: hu97DA8A
name: NAR
date: 2012-12-04
result:
  University of Colorado (UCO001)____________________________________________________________________________Patient Name: Lawrence HunterÂ Â Â Â Â Â Â Â Gender: MaleMRN: 1557542Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â  Date of Birth: 1/18/1961Age: 51Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â A


human_id: hu97DA8A
name: NAR
date: 2011-07-12
result:
  Microscopic Diagnosis:  A) Ascending Colon and hepatic flexure, polypectomies:- Multiple fragments of tubular adenomas B) Colon, splenic flexure, polypectomies:- Fragments of tubular adenomas - Hyperplastic polyp- Fragment of colonic mucosa without histop


human_id: hu97DA8A
name: NAR
date: 2011-07-12
result:
  University of Colorado (UCO001)_______________________________________________________________________________Patient Name: Lawrence HunterÂ Â Â Â Â Â Â Â  Gender: MaleMRN: 1557542Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Date of Birth: 1/18/1961Age: 50Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â


human_id: hu97DA8A
name: NAR
date: 2009-03-13
result:
  DATE: 3/13/2009 at 1335CLINICAL INDICATION: Baseline for grantSTUDY: Stress views of the bilateral handsCOMPARISON: NoneFINDINGS: There is a small ossified density adjacent to the rightulnar styloid that likely represents accessory ossicle. The bones areo


human_id: hu36A1E8
name: NAR
date: 2017-05-16
result:
  XR CHEST PA AND LATERALIndication: screening, Z00.00 Encounter for general adult medicalexamination without abnormal findingsComparison: NoneFindings:Cardiac and mediastinal contours are normal. Small nodules in bilateralupper lungs, likely sequela of pri


human_id: hu36A1E8
name: NAR
date: 2016-01-25
result:
  Study: 3 views of the right foot dated 1/25/2016.Comparison study: 12/2/2011.History:Â Â Pain at the base of the second and third toes.Findings: No acute fractures or dislocations are identified. Bone densityand architecture are age and gender appropriate.


human_id: hu36A1E8
name: NAR
date: 2016-01-25
result:
  Left knee radiographs, 3 viewsClinical information: M25.562 Pain in left knee, pain.Comparison: NoneFindings:No acute fractures or dislocations are identified. Bone density andarchitecture are unremarkable for age and gender. No arthritic changes areappre


human_id: hu36A1E8
name: NAR
date: 2014-04-10
result:
  Study: XR PELVIS 1 TO 2 VIEWS, 2 imagesIndication:789.03 Abdominal pain, right lower quadrant, R groin painComparison:None available.Findings and Impression:No acute fracture or dislocation. Hip joint spaces are preserved. Minimaldegenerative proliferatio


human_id: hu36A1E8
name: NAR
date: 2011-12-20
result:
  Â Â Â Â Â Â Â Â Â Â  CARDIAC DIAGNOSTIC UNITÂ Â Â Â Â Â Â Â Â Â Â Â Â Â  Date: 12/20/2011 13:00:00Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â  AdultÂ Â Â Â  MaleÂ Â  Age: 52Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â  ECHO-DOPPLER REPORTÂ Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â  OutpatientÂ Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â


human_id: hu36A1E8
name: NAR
date: 2011-12-02
result:
  Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â  VerifiedRight ankle pain.Findings and impression: 3 views right ankle. No acute bone, joint, orsoft tissue abnormality. Prominent Stieda&#39;s process incidentally noted.Electronically Reviewed by: John A. Mastrangelo MDElectronic


human_id: hu36A1E8
name: NAR
date: 2011-12-02
result:
  Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â  VerifiedPain right foot.Findings and impression: 3 views right foot. Prominent Stieda&#39;s process.No acute fracture. Incidental note is made of a bipartite tibialsesamoid. Incidental note is made of likely an accessory ossicle a


human_id: hu36A1E8
name: Clinical History
date: 2010-03-09
result:
  Indications:Â Â Screening for colorectal malignant neoplasm, this is thepatient&#39;s first colonoscopy.Impression:Â Â The examined portion of the ileum was normal.Â Â One, 4 mm polyp inthe ascending colon.Â Â Resected and received.Â Â Diverticulosis in the sigmoidcolo


human_id: hu976B29
name: IMP
date: 2015-02-27
result:
  IMPRESSION:1. Normal exam.Â Â Â Â  Â Â  Dictated by: Christina Jacobs, MD on 2/27/2015 4:18 PM.Â Â  Electronically signed by: Christina Jacobs, MD on 2/27/2015 4:18 PM.


human_id: hu976B29
name: IMP
date: 2014-12-05
result:
  IMPRESSION:1.Â Â  Recurrent small bowel obstruction secondary to active Crohn&#39;s disease atmultiple sites in the right lower quadrant.Â Â The thickening and enhancementof the terminal ileum is similar to recent previous exam from February 8,2014.Â Â There are 3


human_id: hu976B29
name: IMP
date: 2014-12-04
result:
  IMPRESSION: Unremarkable soft tissue contours. Nonspecific gaseous distention of bowelthroughout the abdomen. This could reflect ileus or obstruction. Considerfurther evaluation with CT abdomen and pelvis.Â Â Â Â  Dictated by: Ryan Duhn, MD on 12/4/2014 9:37


human_id: hu976B29
name: IMP
date: 2014-02-08
result:
  IMPRESSION:1. Inflammation of the terminal ileum, most suggestive of Crohn&#39;s disease.2. Distal small bowel dilation and dilation of the stomach. The pattern mostsuggests ileus.Dictated by: Joseph Borrello, MD on 2/8/2014 11:57 AM.Â Â  Electronically signed


human_id: hu976B29
name: NAR
date: 2012-10-15
result:
  Michael P Williams, MDÂ Â Â Â  10/15/2012Â Â 9:44 PMHPIReview of SystemsPhysical ExamLumbar PunctureDate/Time: 10/15/2012 7:30 PMPerformed by: VOTAVA, DANIEL HENRYAuthorized by: WILLIAMS, MICHAEL PConsent: Verbal consent obtained. Written consent obtained.Risks


human_id: hu976B29
name: IMP
date: 2012-10-15
result:
  IMPRESSION:Â Â Â Â 1. Normal chest.Â Â  Â Â Â Â 2. No change.DICTATED BY: Hodgman MD, C. Gregory ELECTRONICALLY SIGNED BY: Hodgman MD, C. Gregory ELECTRONICALLY SIGNED ON: 10/15/2012 17:09:54


human_id: hu976B29
name: IMP
date: 2012-10-15
result:
  IMPRESSION:Â Â Â Â 1. No acute intracranial abnormality.Â Â Â Â DICTATED BY: Oostveen MD, Robert ELECTRONICALLY SIGNED BY: Oostveen MD, Robert ELECTRONICALLY SIGNED ON: 10/15/2012 16:48:40


human_id: hu976B29
name: NAR
date: 2011-05-23
result:
  BRONSON DEPARTMENT OF RADIOLOGY  KALAMAZOO, MICHIGAN  ORDER: CT ABDOMEN PELVIS W CON  PATIENT: PEER, JONATHAN GERARD  HOSPITAL NUMBER: B0012987574  ACCOUNT NO: 1114300268  SEX: M  DOB: 09/27/1982  ADMISSION DATE: 05/23/2011 09:14  CHECK-IN NUMBER: 2372768


human_id: hu976B29
name: NAR
date: 2011-05-23
result:
  BRONSON DEPARTMENT OF RADIOLOGY  KALAMAZOO, MICHIGAN  ORDER: XR ABDOMEN ACUTE  PATIENT: PEER, JONATHAN GERARD  HOSPITAL NUMBER: B0012987574  ACCOUNT NO: 1114300268  SEX: M  DOB: 09/27/1982  ADMISSION DATE: 05/23/2011 09:14  CHECK-IN NUMBER: 2372570  PT TY


human_id: hu976B29
name: NAR
date: 2011-01-24
result:
  BRONSON DEPARTMENT OF RADIOLOGY  KALAMAZOO, MICHIGAN  ORDER: XR SMALL BOWEL  PATIENT: PEER, JONATHAN GERARD  HOSPITAL NUMBER: B0012987574  ACCOUNT NO: 1101801258  SEX: M  DOB: 09/27/1982  ADMISSION DATE: 01/24/2011 07:48  CHECK-IN NUMBER: 2298778  PT TYPE


human_id: hu75F3D7
name: Demographics
date: 2015-11-30
result:
  ** DEMOGRAPHICS DRAWN FROM PATHOLOGY REPORT **PATIENT:Â Â  HALL, MELISSA CARRELLMRN:Â Â Â Â Â Â  H3778323Â Â Â Â  (HMC)DOB:Â Â Â Â Â Â  Jul 28 1976SEX:Â Â Â Â Â Â  F.CASE:Â Â  CG-15-14295Â Â  COLLECTED:Â Â Nov 30 2015Â Â RECEIVED: DecÂ Â 1 2015


human_id: hu75F3D7
name: Demographics
date: 2015-11-30
result:
  ** DEMOGRAPHICS DRAWN FROM PATHOLOGY REPORT **PATIENT:Â Â  HALL, MELISSA CARRELLMRN:Â Â Â Â Â Â  H3778323Â Â Â Â  (HMC)DOB:Â Â Â Â Â Â  Jul 28 1976SEX:Â Â Â Â Â Â  F.CASE:Â Â  MX-15-07506Â Â  COLLECTED:Â Â Nov 30 2015Â Â RECEIVED: DecÂ Â 1 2015


human_id: hu7FC773
name: Factor V Leiden Mutation
result:
  Result:  Negative (no mutation found)
                                                             .
  Factor V Leiden is a specific mutation (R506Q) in the factor
  V gene that is associated with an increased risk of venous
  thrombosis. Factor V Leiden is more


# procedures

human_id: hu1BD549
date: 2010-02-04
name:
  Transvenous Electrode Insertion - For Permanent Pacemaker or Pacing Cardioverter-Defibrillator, Dual Chamber


human_id: huF8FDDF
date: 2012-12-20
name:
  COLONOSCOPY, FLEXIBLE, PROXIMAL TO SPLENIC FLEXURE; WITH ABLATION OF TUMOR(S), POLYP(S), OR OTHER LESION(S) NOT AMENABLE TO REMOVAL BY HOT BIOPSY FORCEPS, BIPOLAR CAUTERY OR SNARE TECHNIQUE


human_id: huF8FDDF
date: 2012-05-31
name:
  RADIOLOGIC EXAMINATION, ABDOMEN; COMPLETE ACUTE ABDOMEN SERIES, INCLUDING SUPINE, ERECT, AND/OR DECUBITUS VIEWS, SINGLE VIEW CHEST


human_id: huF8FDDF
date: 2012-04-20
name:
  COLONOSCOPY, FLEXIBLE, PROXIMAL TO SPLENIC FLEXURE; WITH REMOVAL OF TUMOR(S), POLYP(S), OR OTHER LESION(S) BY SNARE TECHNIQUE


# survey

human_id: hu4A2DC0
date: 2011-07-15 19:08:04
phenotype: Yes
phenotype_category:
  Participant_Survey:Have you uploaded health record data using our Google Health or Microsoft Healthvault interfaces?


human_id: hu831FD6
date: 2011-07-15 19:27:25
phenotype: Long QT Syndrome
phenotype_category:
  Participant_Survey:Do you have a severe genetic disease or rare genetic trait? If so, you can add a description for your public profile.


human_id: huD09050
date: 2011-07-15 19:28:37
phenotype_category:
  Participant_Survey:Do you have a severe genetic disease or rare genetic trait? If so, you can add a description for your public profile.

phenotype:
  1. Extreme susceptibility to motion sickness. - answers pertain to this trait\n2. Pyloric stenosis\n3. Unusually small feet for my height


human_id: huDFBF54
date: 2011-07-16 02:52:38
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  Too much to describe --- but perhaps my listing of IDDM (insulin dependent diabetes ...) is a stretch as it is only thought to be partially genetically driven ...


human_id: hu3BE6EF
date: 2011-07-16 09:23:56
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I inherited Autosomal Dominant Polycystic Kidney Disease (ADPKD) from my father, as did two of my siblings. I learned recently that I also have a very mild form of Von Willebrand Disease.


human_id: hu3BE6EF
date: 2011-07-16 09:23:56
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  I'm part of a study -- taking an experimental drug called Tolvaptan that may prove successful in treating PKD. As part of that study, an MRI of my kidneys is taken once a year. Perhaps that MRI could be uploaded.


human_id: hu04A590
date: 2011-07-16 10:21:47
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I can wiggle my ears.  My father could also wiggle his ears.  I remember that, as a small child, after having seen him do this once to make me laugh, I tried it and had no problem wiggling my own ears, so I am guessing this is an inherited trait rather than a learned ability.


human_id: huC4A276
date: 2011-07-16 10:56:08
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Gluten intolerance - I am unaware of anyone else in my family having this disorder.  I do not have the known genetic profile for celiac however I have a profound intolerance that mimics celiac.  I would guess that it is genetic but that the genetics are unknown.\n\nAlzheimer's - I do not display symptoms, at this time my mother doesn't display symptoms, she is 67, her sister (my aunt has symptoms starting around 70).  My grandmother had symptoms staring in 50s.  She had 5 siblings that made it to adulthood, one sister had symptoms starting in her 50's, one had symptoms in his 70s,  the other two did have symptoms that I know of.  My aunt who has symptoms currently has 4 children, I do not know if they would be interested in PGP, but I would be willing to ask them.  \n\nHigh Cholesterol, not rare but probably genetic, my sister has it as does my mother.


human_id: huE2E371
date: 2011-07-16 11:20:08
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  orthostatic hypotension: under continuous treatment * described below\npsoriasis: under continuous treatment\nocular melanoma: treated June 2006 by Plaque Radiation\nthyroid papillary carcinoma - follicular variant: complete thyroidectomy Dec 2010


human_id: hu5C3F07
date: 2011-07-16 11:50:21
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Carrier of 2 ApoE4 alleles (significantly increased risk for late-onset Alzheimer's disease). \nCystic fibrosis carrier (CFTR gene mutation).


human_id: huBA2A39
date: 2011-07-16 11:50:43
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  MS diagnosed in 1990 as Chronic Progressive\nLow blood formation also known as "pre-lukemia" diagnosed in 2009


human_id: huBA2A39
date: 2011-07-16 11:50:43
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  A series of MRIs every 2 years from diagnosis (do not have original test) to present.\nBlood test results and cyto test (I will provide true name on request - I just cannot remember the correct name just now)


human_id: hu433D3A
date: 2011-07-16 11:59:31
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  1) Morbid Obesity (note: age of onset hard to pin down as I was a weight cycler.  Worst after 50, however)\n\n2) Need peace and quiet


human_id: hu61C43A
date: 2011-07-16 11:59:42
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  The rare trait that I believe to have some genetic component is being transgender. While this condition is very rare and has been little studied, I am very willing to be a part of discovering the whys and wherefores of this trait.


human_id: hu92FD55
date: 2011-07-16 12:30:40
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Father over age 35: Increases chances of genetic mutation.\n\nAnyways, I seem to have a uniquely severe case of combined Asperger's+ADD that doesn't exactly totally map with the symptoms mapped by the DSM-IV. And for whatever reason, I'm very strongly novelty-seeking.\n\nPersonality-wise though, people say that I'm the most unique person that they've ever met. \n\nAlso, I seem to have a very strong sensory hypersensitivity issue (I go to all sorts of doctors but none of them seem to have any ideas about it).


human_id: hu6AE31C
date: 2011-07-16 12:34:58
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I don't know if this is 'rare enough,' but I am the only one in my family with red hair & freckles- my mother is Danish & my father has Spanish origins.


human_id: hu144601
date: 2011-07-16 12:41:48
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  I have had Celiac Blood Panel done and also an endoscopy with biopsy done on small intestine/jejunum.


human_id: huAA53E0
date: 2011-07-16 12:51:32
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I believe several traits are genetic in nature\n\n1. "Blue rubber bleb nevus syndrom" connected to TEK tyrosine kinase mutation (http://en.wikipedia.org/wiki/Blue_rubber_bleb_nevus_syndrome) \n\n2. Narcolepsy and "Delayed sleep phase syndrome" \n\nThere are a few more but I believe these two are the easiest to focus on.


human_id: huAA53E0
date: 2011-07-16 12:51:32
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  I have a letter from the oncologist at OCB (Ophthalmic Consultants of Boston) to my PCP describing this condition (BRBNS)


human_id: huA872A6
date: 2011-07-16 12:57:56
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Severe life-long depression; all of my sibs (5) have it and my mother but not my father.  I will answer the following questions about this one.\n\ncleft palate without cleft lip\n\nwhite forelock


human_id: huD7960A
date: 2011-07-16 13:03:26
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have a disorder that falls within the phenotype of a severe form of hypokalemic periodic paralysis. It seems to have an autosomal dominant pattern on my father's side of the family, and includes daily weakness and loss-of-consciousness episodes coming from food.  For me, there is also documented full-body paralysis including full breathing paralysis (causing an emergency) and many other abnormal and severe reactions to many common hospital medications. \n\nLike other forms of hypokalemic periodic paralysis, the age of onset of the symptoms for me was at 20 years of age. The next generation in the family is now beginning to be affected. Unlike other forms of PP, my symptoms include cardiac symptoms, CNS symptoms and pancreatic symptoms, all in response to food. There are many severe medication reactions, of course.\n\nI have had genetic tests for the most common genes for periodic paralysis, but these tests were negative, likewise negative tests for the common pseudocholinesterase deficiency genes.\n\nI have been told that the cause is most likely a "medically new" channelopathy. If so, it is currently undiscovered.\n\nMy own feeling is that the disorder is more severe for me because of the effects of several genes, not just one gene. In particular, I suspect the main abnormality is in genes that are directly or indirectly involved in the potassium ATP channels, which could explain why I have such severe symptoms.\n


human_id: huD7960A
date: 2011-07-16 13:03:26
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  1. I have a letter from the anesthesiologist who describes one of my paralytic reactions that caused breathing paralysis, and what he did about it. \n\n2. I have EKG's from a Holter test that document unusual cardiac reactions. Before eating, the EKG looked very good and the heart rate was 60 bpm. After eating, tachycardia took place, where the resting heart rate rose to 128 bpm and there were many arrhythmias and irregularities. The EKG's didn't even look like EKG's anymore. The episodes lasted for about 5 hours, slowly subsiding almost to normal again at the end, but then it was time for the next meal. Because there were three meals, about five hours apart, there were fifteen hours of abnormal EKG patterns, all subisiding by the end of the 5 hour interval, recorded on the Holter.\n


human_id: hu61CF9B
date: 2011-07-16 13:15:05
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I am diagnosed with Asperger's Syndrome (Autism Spectrum Disorder). I have a clinical diagnosis from an autism specialist here in New York City. I have also participated in several brain imaging studies in Boston. I have a research diagnosis of Autism Spectrum Disorder. I was given the ADOS and my mother was given the ADI in order to qualify me for a study. My autistic disorder has affected my ability to work and establish social relationships.


human_id: hu61CF9B
date: 2011-07-16 13:15:05
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  MRI of brain. \nLetters from researchers describing results of tests (with identifying parts redacted).\nResults of IQ test.\nResults of ADI/ADOS tests.\nResults of other miscellaneous studies I had been in.


human_id: huD37D14
date: 2011-07-16 13:25:07
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have an autoimmune disease which was first diagnosed as Crohn's. It has manifested in other symptoms diagnosed as Sjogren's and Vitiligo both of which my sister also has.\n\nMy sister and I both have the HLA-B27 antigen, which i have been told is rare for caucausians, I have also been + for the rare RNP antigen which I've been told is indicative of Connective Tissue Disease, though it is not yet active (I was just tested last year and was negative, but told that it fluctuates when inactive).\n\nWhen active, this disease is severe and often fatal. Right now, I am battling constant fibromyalgia-like pain and arthritic pain but am monitored.


human_id: huD37D14
date: 2011-07-16 13:25:07
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  Have some lab results from Kaiser for antigens (not latest -RNP result) also any Colonoscopy/pathology reports if needed for Crohn's diagnosis. Have additional records for abnormal Bravo pH study prior to Nissan Fundiplication surgery for GERD. Also, visit summary from a Rhuematology specialist post RNP+ (pre-vitaligo). Can obtain dermatology reports if necessary.


human_id: hu162513
date: 2011-07-16 13:26:47
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Stroke, with associated hypertension.\nI had a stroke at age 50, my father had it at the same age, but pasted away from a traffic accident. My uncle (father’s brother) and my father's first cousin past away from a stroke at 52.


human_id: hu263CFD
date: 2011-07-16 13:31:16
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have two diseases that I believe have a strong genetic link.  The first is psoriasis on my hands and feet, that goes into remission for years and then reappears.  This is the condition I will use for answering the questions below.  \n\nThe other condition which may have a gnitic component is super ventricular tachycardia.


human_id: hu3A1B15
date: 2011-07-16 13:32:40
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have an expanded CAG repeat of 37 in the huntingtin gene, but am asymptomatic (at age 37). CAG repeats of 40 and above are fully penetrant for Huntington's Disease (HD), a rare, fatal neurodegenerative, autosomal dominant disease for which there currently exists no treatment. Although the most common age of onset for HD for those with 40 or more CAG repeats is the 30s, age of onset varies considerably and is inversely correlated with number of CAG repeats. That said, the number of repeats does not account for all of the variation in age of onset, and the conventional wisdom is that secondary genes likely account for the remaining variation.\n\nCAG repeats between 35 and 39 (roughly) are associated with reduced penetrance. While clinical HD is rare, "intermediate range" HD alleles, both expressed and unexpressed, are even rarer, at least as represented in the clinic and in the literature. When I was tested, circa 2002, predictions about probability of developing HD within a normal lifetime were based, for each allele in the 35-39 range, on an n of a handful individuals. Based on that data, I was told that the 37 allele confers roughly a 50% chance of developing HD within a normal lifespan, with age of onset varying considerably among the handful of known symptomatic individuals, from the early 30s to the 80s. That said, more recent research questions the basis on which these predictions were made. It's likely that those with intermediate range alleles who are symptomatic or whose relatives (with whom they share secondary genes that may influence penetrance) are symptomatic are probably overrepresented (relative to others carrying an intermediate range allele) in the clinic and, thus, in the data. The incidence of intermediate CAG expansion is almost certainly much higher than the literature suggests, and may be higher than the incidence of 40+ CAG expansion, especially given the possibility of de novo mutations.\n\nThe parent from whom I inherited this allele also has a 37, is also asymptomatic (at age 62), and has expressed interest in participating in genetic research that may advance knowledge about HD. This parent was also comfortable undergoing partial sequencing (not, of course, including the huntingtin gene) through 23andMe. \n\nThe grandfather from whom I inherited the allele was asymptomatic for HD upon death (in his early 80s), per clinical evaluations and as confirmed through analysis of brain tissue samples sent to MacLean's (the tissue showed one of the most advanced cases of Alzheimer's-related atrophy, etc. they had ever seen, but no signs of HD). That sample, sent around 2000, may still be available.\n\nMembers of my extended family have various fully-penetrant alleles (e.g., 45) and to date one member has died from HD. But they would not be interested in participating in the PGP.


human_id: hu7DE7FD
date: 2011-07-16 13:33:23
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  Multiple Sleep Latency Test, negative other tests that rule out other causes of excessive daytime sleepiness, possibly EEG (not sure what format it is in or how accessible it is -- will ask my doctor).


human_id: hu5E3BEB
date: 2011-07-16 13:40:15
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Hypospadia, undescended testicles, micro penis I have two 1st cousins and 1 nephew that have 1 or more of these traits. All of us required surgery to correct. None are interested in being part of the PGP. This is the one I am continuing the survey on.\n\nI also had 2 bouts of spontaneous collapsed lung (left) and I have 1 1st cousin that also had this. He is also not willing to be part of the PGP. I underwent surgery he did not.


human_id: hu76CAA5
date: 2011-07-16 13:59:12
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Paroxysmal atrial fibrillation with rapid ventricular response. I have had three emergency electrical cardioversions for the condition, but I have been free from recurrences since starting the extended release form of propafenone (325 mg capsule BID). My maternal grandfather died from stroke at about age 72 in the early 1960s in rural Texas, & was being treated with digitalis for a diagnosis that we do not currently have on record. My mother's fraternal twin sister has been off & on coumadin for atrial fib, & my mother, myself & several others in the family show a 33.9% risk for atrial fib projected by 23andMe. The inheritance pattern is clearly my maternal line.


human_id: hu76CAA5
date: 2011-07-16 13:59:12
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  Cardioversion records are available in my Google Health account, & I have already made my 23andMe raw data available to the PGP.


human_id: huE3FDE9
date: 2011-07-16 14:01:08
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Severe depression, diagnosed as Bipolar disorder.  My mother was institutionalized, my brother committed suicide last year, and I am on Disability and unable to work or function normally in society, even with intensive therapy and medication.


human_id: huBAA265
date: 2011-07-16 14:01:50
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I am chronically ill and believe that I have several conditions that are genetic in origin, however I will complete the remaining questions with my answers relating to the Porphryia.  I'm only going to list the disease I consider to be relatively rare below (although I also have hypothyroidism, heart disease, gallbladder disease, fibrocystic breasts, upper airway resistance syndrome, ablated Wolfe-Parkinson-White Syndrome and an ectopic kidney):\n\n-Porphyria (probably Erythropoietic protoporphyria or Hereditary Coproporphyria) (undetected by Mt. Sinai genetic study)\n-Phenol sulfotransferase deficiency\n--Congential Nonspherical Hemolytic Anemia (in remission)


human_id: huE7765D
date: 2011-07-16 14:11:45
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Blod cloth formation without any obvious reason.  Pulmonary embolism.  One of my first cousin died because his blod coalugated all over in his body.


human_id: huFABE5E
date: 2011-07-16 14:43:40
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  My family history has significant auto-immune disease.\n\nCeliac Sprue: father and sister - Hypothyroid: father and me - Dairy allergy: nephew and me - Rheumatoid arthritis:  mother (very severe and active for decades) - Diabetes:  son - Kidney failure: father (no alcoholism or drug use) -Pernicious anemia: father and mother\n


human_id: hu7D6AB1
date: 2011-07-16 14:54:45
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I had no risk factors for a coronary disease, however, out of nowhere, in August 2009, I discovered that I had 6 blockages in the 3 main arteries going to the heart. As a result, I had to have a triple bypass operation. It was totally successful and I am fine now. the doctors were extremely surprised to see that and could only say that it must be genetic since my mother had heart disease.


human_id: hu1BD549
date: 2011-07-16 15:33:59
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have several genetic diseases, some rare some common:\nLong QT syndrome (some of the variants causing this (~75%) have been identified.  I have a variant but it is a new one that has not been confirmed.\nType 1 Diabetes\nAntiphospholipid antibody syndrome\n(Both autoimmune disease, linked to SNPs in the HLA region of Chr 6)


human_id: hu1BD549
date: 2011-07-16 15:33:59
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  LQTS: genetic tests performed by GeneDx and EKG interpretations\nAutoantibody test results for T1DM and APS


human_id: huF83462
date: 2011-07-16 16:06:46
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  I was diagnosed and am being treated at Stanford University Movement Disorder Clinic. \nI can ask them for documentation


human_id: huF160AA
date: 2011-07-16 16:12:22
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Long term non-progressor for HIV - 25 years without antiviral medication\nHLA B35 allele \nHeterozygous CCR5  Delta 32 deletion\n


human_id: huF160AA
date: 2011-07-16 16:12:22
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  Results of blood tests for CD4/CD8 counts, HIV,  genetic HLA typing etc.  CD4/CD8 count history dates from 1986 - present\nYou may also want to request results from any of the several research studies in which I participate as they have more detailed information\n\nDr. Jay Levy  at UCSF\nSCOPE at S F General Hospital\nHIV Elite Controller research at NIH/NIAD in clinic OP8 - Dr. Mark Connors / Dr. Steve Migueles\nHIV Elite Controller research at MGH - Dr. Bruce Walker / Ragon Institute


human_id: hu016B28
date: 2011-07-16 16:12:50
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Cervical Spinal Stenosis (required laminectomy and fusion from C2-T1).  It was a congenital narrowing that manifested with symptoms in my mid-30s.


human_id: hu174334
date: 2011-07-16 16:17:09
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Severe-Squamous cell cancer (SCC) x9 (skin), after Stevens Johnson Syndrome (SJS), right groin hematoma became SCC.  Surgeon believes SSC from SJS with 2 surgeries, chemo and radiation, and if so could be Muir Torre or Lynch Syndrome and both are genetic.  My mother (jaw-mandible, tongue) and her sister (pelvic) both had SCC. Age 78 acquired for me.\nCongenital trait-I was born with 6 fingers, my sister, 6 fingers and 6 toes (deceased) and my younger brother 3 nipples (deceased). I also have 1 extra cervical rib.\nCongenital- father-severe scoliosis- I have mod. cervical 5-6, lumbar 4-5, 2 of my children have mild.  I have one niece who has one child has scoliosis and had rod placement several years ago.


human_id: hu174334
date: 2011-07-16 16:17:09
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  Diagnosis-Stevens Johnson Syndrome 10/2009 following severe drug reaction to Septra DS, with 2 hospitalizations, several PET scans and ultrasound showing hematoma right groin 2008, 11/09 DVT and right groin adenopathy, surgery 3/10 right groin SCC, 4/10 neg. Pap, 8/10, small Basal Cell Cancer removed from right scapula (pustule from SJS Hx) 7/10, another right groin SCC, 8/10 VAIN 3, 12/10, negative PET scan, 6/11-neg Pap.


human_id: hu42CA7C
date: 2011-07-16 16:37:55
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  I am 55 years of age and have lab results for my cholesterol that go back to age 20 since I worked in a clinical lab. My total cholesterol and LDL levels are typically sky high - above 300 mg/dl.  And my HDL levels are moderately low, below 50 mg/dl. Not conferring on me the numerical protection normally associated with high HDL levels. Despite this I have no apparent cardiac myopathy or artherosclerosis normally associated with such high levels. This means there are more cards in the cholesterol game than we currently understand. My high levels remain relatively untreated due to the fact that statin drugs give me instant tendonitis, also likely a genetic trait.


human_id: hu351AF9
date: 2011-07-16 17:31:37
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  autoimmune diseases\neyeritis\nlikely Rheumatoid Arthritis\nCyst in the Ankle\ncontct dermatitis\nvitiligo\nleft orvhiectomy


human_id: huEEE6E8
date: 2011-07-16 17:46:51
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  The rare trait is transient mild Alopecia Areata, which I am hoping to tested as part of the MJF project.


human_id: huD81276
date: 2011-07-16 18:49:16
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  There seems to be a strong propensity in my family toward bipolar disorder, depression, and chronic substance abuse. Many family members died at young age connected with this. I have been treated for mental illness myself and some of my children have issues with this as well


human_id: hu99967E
date: 2011-07-16 19:56:12
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  During a full Sequence of my mtDNA it showed a mutation known as "heteroplasmy."  My heteroplasmy mutation is listed as 16368T/C.


human_id: hu4C20BC
date: 2011-07-16 21:09:07
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have had two episodes (for three years starting at age 13, and an ongoing episode beginning at age 23) of severe depression. Other family members have been diagnosed with or have exhibited clear symptoms of the disease.


human_id: hu4C20BC
date: 2011-07-16 21:09:07
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  I would be willing to make a psychiatric evaluation and a medication history available on my public profile.


human_id: hu6D1115
date: 2011-07-16 21:47:13
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  high homocysteine\n\nthe answer below is when I first became aware of it as a result of my father's heart attack.


human_id: hu6D1115
date: 2011-07-16 21:47:13
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  Last year I was tested by a pediatric geneticist at UCLA who specializes in the condition in newborns. It was determined that I am hetrozygous for the MTHFR C677T variant. Many years prior to that my father's cardiologist reported that he had the highest homocysteine ever seen by a lab in Western Canada and recommended that he tell his offsprings to be tested for the condition. My homocysteine level was found to be quite high though it has subsequently been reduced by treatment. I have entered both my initial and my current homocysteine levels in Google Health.


human_id: hu868880
date: 2011-07-16 21:54:55
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Though I am only 52, I have experienced a number of significant medical issues that may well be characterized as rare or severe:\n\nAt 28 I was diagnosed with massive brain bleed and underwent a craniotomy for a partial resection of my left parietal lobe.  Though there was a significant loss of brain due to both the bleed and surgery, there were no obvious neurological after effects, leading my neurologist to conclude that the bleed was congenital (AVM) and had been present since birth, resulting in constant small damage, and allowing my brain to rewire itself as it developed (rather than the trauma that would result if the same area of my brain were damaged in adulthood all at once.\n\nAt 47 I was diagnosed with Kidney Cancer (renal cell carcinoma) via an incidental finding during an appendectomy follow-up.\n\nAt 48, while recovering from the Kidney Cancer surgery, I began to have movement difficulties and was eventually diagnosed with a 6.5cm meningioma that was removed via craniotomy (and was located proximate to the previous AVM surgery) - subsequently additional small tumors (also meningioma or perhaps schwanoma) have been discovered via imaging.\n\nAnd last, but not least, I am transgender (MtF), an awareness I have had since I was approx. 2 years old (and well before I had the vocabulary or analytical tools to understand what it meant.)


human_id: hu868880
date: 2011-07-16 21:54:55
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  With respect to my meningiomas, I underwent an NF2 test (which turned out to be negative), but I have all of my brain MRI's available as DICOM files, showing both the meningiomas as well as the 'hole' left from the AVM resection. I would also be willing to share my doctor's notes\n\nWith respect to my kidney cancer, i have CT scan files available as DICOM files, and would also be willing to share my doctor's notes.\n\n


human_id: huBEDA0B
date: 2011-07-16 22:14:51
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Vascular hemangiomas ( several family members have these)\nbenign breast lumps ( my mother had them. - about 8 surgically removed)


human_id: huBEDA0B
date: 2011-07-16 22:14:51
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  I have bunch of records including surgeon's report5)-5 I should have sent to you.  I will se if I can find them.


human_id: huA33758
date: 2011-07-16 22:31:28
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have extra processes on my clavicles, as well as mandibular tauri, both of which traits my mother and sister also have.


human_id: hu5917F3
date: 2011-07-17 00:21:11
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  I have had MRIs and spinal fluid analysis to confirm diagnosis of Multiple Sclerosis and also several followup MRIs to follow progress of the disease.  I do not have the MRI films or lab results in my possession, but they are available and I believe I can request copies of them if that would be advantageous to the project.\n


human_id: hu4D474D
date: 2011-07-17 00:55:57
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I'm not sure if this counts as a rare trait but I'm gay and I believe that being gay has a strong genetic connection.


human_id: hu3B8141
date: 2011-07-17 03:03:56
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Atrial Node growth causing atrial fibrillation. I recently had a MAZE procedure to ablate and isolate the extra nodes as well as left atrial appendage removal.


human_id: hu005725
date: 2011-07-17 03:55:33
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Depression and possible bipolar disorder. Males especially over generations have had this.\nAlso Meniere's disease, idiopathic, but many family members have it so who knows.\nThyroid disease is also rampant in my family, virtually all females have it, some males.


human_id: hu5B337F
date: 2011-07-17 05:55:21
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I consider my homosexuality to be a genetic trait. Most data that I have seen and read points to sexuality being genetic, and I know for sure that I made no choice in acquiring it. As this means the most to me, the answers will pertain to this.\n\nBipolar disorder. As far as I know this is both genetic and environmental. I have never been professionally diagnosed, but I have talked with professionals who agreed with my diagnosis.


human_id: huDA2757
date: 2011-07-17 07:19:09
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Multiple:\n\nMy IQ consistently tests over 160, and typically in the 170-180's, for spatial skills and mathematic comprehension.  Verbal ability is within the high end of "normal".\n\nI also have "atrial branch delay" as described by a cardiologist.  I have relevant medical data and testing information for this, but even with my EMT certification, this issue is too specific for me to describe after reading the information.  A cardiologist would have to comment on this further.  From what I understand, this is a rare, but trivial, electrical defect in the heart.\n\nFurther, I have recently been diagnosed with migraines, which apparently affects <1% of adult males.\n\nAnd finally, I was tested at age 18 to have 115% of normal tidal volume for my external body measurements, and have been able to achieve a *standing* heart rate of 40 beats per minute due to exercise alone.


human_id: huDA2757
date: 2011-07-17 07:19:09
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  Mensa test results for IQ.\n\nAnd, for heart information, all medical information should still be on file at the cardiologist's office to include NMRI, holter moniter data, echocardiogram video, stress test and EKG.


human_id: hu78E6A9
date: 2011-07-17 10:01:31
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Amyblyopia: vision uncorrected is 20/200 in one eye, 20/50 or better in the other. My father has the same.


human_id: hu78E6A9
date: 2011-07-17 10:01:31
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  I could easily provide prescription for corrective lenses. I would not mind sharing records from my opthalmologist but would have to pursue gathering these.


human_id: huA0E089
date: 2011-07-17 11:10:50
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have facioscapulohumeral muscular dystrophy or FSHMD. There are 4 generations known in my family who have the disease.  I have lupus anticoagulant.  It is kind of a misnomer because it has nothing with lupus eryrathematosis.


human_id: hu838AF4
date: 2011-07-17 11:27:18
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have Factor XI deficiency, formerly known as  hemophilia C. It is thought to occur in 1 in 100,000 people, and mostly in those of Ashkenazi jewish descent (there are no such known people in my genetic family history).


human_id: hu838AF4
date: 2011-07-17 11:27:18
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  I have had my Factor XI levels measured and they are 50% of normal. I was tested because my daughter was found to have this same condition.


human_id: huA4E2CF
date: 2011-07-17 11:30:22
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  I do not have the x-ray in my possession however I am willing to provide such through my medical provider.


human_id: hu77CC58
date: 2011-07-17 12:23:12
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Diagnosed with a rare CNS tumor: myxopapillary ependymoma of the filum terminale.  Incidence one in a million per year, roughly.  The tumor was present from the age of 18 or earlier.  Successfully removed at age 27.


human_id: hu27FD1F
date: 2011-07-17 13:19:37
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Autosomal dominant non-syndromic progressive sensorineural hearing impairment. It is detectable in early childhood and progresses gradually to the point where cochlear implants are indicated in older family members.\n\nOur extended family has participated in several genetic studies, but the gene has not been identified. By testing at 23andMe for six relatives with the impairment and several without, I have been able to narrow down the region to about 16Mb on chromosome 15. I also have father/mother/child data for phasing and I can identify the haplotype. None of the 50+ genes currently implicated in hearing loss are found in this region, and in fact, no genes clearly identified with hearing function in general. Identification of the mutation in our family would thus contribute to the understanding of genes important for normal function.


human_id: huC9ADBC
date: 2011-07-17 14:38:27
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  Blood measurements of multiple types of thyroid hormones.\nWhite blood cell count.\nLiver enzyme tests.\nCholesterol tests.


human_id: huF09EFF
date: 2011-07-17 20:46:45
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Extremely high cholesterol and triglycerides.  Max readings are around 600 chol and 1500 trig.  Normal being <200 chol and 150 trig.


human_id: huAA67BC
date: 2011-07-17 21:25:13
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I was born with a hereditary geniospasm (quivering chin) that every male in my patrilineal family has had. My father, grandfather, great uncles and other members have all shared this trait.


human_id: huAA245C
date: 2011-07-17 22:07:33
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I've had a craniopharyngioma (2 years ago), Juvenile Rheumatoid Arthritis (until age 8), and dextrocardia (right-sided heart)


human_id: hu4D4061
date: 2011-07-18 01:06:53
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  My diagnosis is Chronic Daily Migraine (possibly New Daily Persistent Headache).  My recollection is that I got a headache as a child that never went away.  I have had some level of headache pain every second of every day since the age of 13.  The pain escalated and has been extremely debilitating from age 33 to now, age 45.  On the paternal side of my family, autoimmune diseases are common.  My PGM , while in her 30's, developed severe rheumatoid arthritis, and all of her children seeminly have autoimmune issues.  My father has allergies, asthma, and atrial fibrillation.  My paternal aunt has Raynaud's Disease and allergies.  My paternal uncle has MS.  Another aunt has eczema and cancer.  There is one paternal, female cousin who is older than I am, and she has either chronic fatigue or fibromyalgia.


human_id: hu4D4061
date: 2011-07-18 01:06:53
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  I have my military childhood health records documenting the onset of the illness.  I have been approved by Social Security for disability.  I have MRIs and blood tests.  I have been treated by several prominent neurologists.


human_id: huB3255F
date: 2011-07-18 01:43:55
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  bloodwork demonstrating chronically low levels of platelets. \n\nalso previous generations of my family have had genetic testing and were written up in the annals of internal medicine in 1981, for being the "first documented case of familial autoimmune thrombocytopenic purpura with bound platelet antibody" and i could upload that article as well.


human_id: huC170B1
date: 2011-07-18 03:26:59
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Reciprocal genetic translocation  of 1st and 4th chromosomes, \nkaryotyped at birth, no apparent signs of translocation manifesting in health.


human_id: huE2A55D
date: 2011-07-18 07:05:21
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Rheumatoid Arthritis.  I was diagnosed several years ago, and I am told that researchers think there may be a genetic element to this and other autoimmune diseases.


human_id: huCE415E
date: 2011-07-18 11:07:48
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have Gilbert syndrome, I had a cousin with Tey Sachs disease, My father died of Spontaneous idiopathic CJD disease, I an an Russian Jewish origins. I will answer for Gilbert disease


human_id: hu86AA7A
date: 2011-07-18 11:26:04
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  My mother's mother died from a liver cancer. My mom died from stomach cancer. Now I have a fatty pancreas and a fatty liver disease.


human_id: hu27E03F
date: 2011-07-18 11:43:56
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Factor V Leiden genetic trait (heterozygous) resulting in more naturally clotting blood - previously unknown but partially resulted in aphasic stroke April 2011.


human_id: huAF34E6
date: 2011-07-18 13:33:44
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  I have report from geneticist on the Ehlers Danlos Syndrome and Chromosome 2p16.3 microdeletion.  I have an Micro CGH and DNA fingerprinting.


human_id: hu12ECE1
date: 2011-07-18 15:09:13
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  non-24-hr sleep wake cycle, very rare, very severe, puberty-onset of symptoms,  formally diagnosed, also present in living father who is also willing to participate in PGP.   \n \nhypothyroidism, common, low \ndepression, common, severe\nanxiety, common, severe\nagoraphobia, uncommon, severe\nanswers are for first.


human_id: huDDD6BF
date: 2011-07-18 15:13:20
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  I have blood tests documenting increased TSH levels and antibody levels.  I also have ultrasounds of my thyroid.


human_id: hu4339C0
date: 2011-07-18 20:36:17
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Since 1955 I've had a chronic eye inflammation first described as iritis, but subsequently as uveitis, peripheral chorioretinitis (sp), and now pars planitis, which I understand to be relatively rare.  I suspect that it is at least partially genetic, with not much evidence other than that another autoimmune condition, vitiligo, appeared within the last decade or so.


human_id: hu72110E
date: 2011-07-18 23:08:04
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  1.) inability to taste bitterness (?TAS2R38 SNP?)\n2.) distal end of thumb's metacarpal square-ish, resulting in limited mobility in the metacarpophalangeal joint


human_id: hu858347
date: 2011-07-19 17:46:35
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I'm afflicted/blessed with the debilitating but possibly incredibly lucrative trait of entrepreneurship, which is only estimated to be apparent in 0.35% of the population. I personally have been very curious as to the likely genetic component of this trait.\n\nI also started getting grey hairs at the age of 19. I'm not sure how rare this is but I'm sure there is a lot of money in this kind of research. Perhaps it could also help with hearing-loss genetic studies (inner ear hair cells failing?).\n\nI also have raynaud's, which is relatively uncommon, being present in 5% of males.\n\nAll of my wisdom teeth grew in with plenty of space. Again, not sure how rare this is.\n\nFinally, I'm a super-taster (25% prevalence).


human_id: huF65A1C
date: 2011-07-19 22:15:29
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  My son had a chest operation to correct the pectus.  I suspect we still have some of the medical records and xrays.


human_id: hu3F83D2
date: 2011-07-20 04:35:24
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  ADHD; Homosexual; HIV+; Left-Handedness; Sina-atrial arrhythmia. Going forward, I'll be answering questions with regards to HIV.


human_id: hu8D1A62
date: 2011-07-20 14:36:22
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  - left-handed\n- photic sneeze reflex\n- palmoplantar hyperhydrosis (referred to in subsequent questions)


human_id: hu616CCD
date: 2011-07-20 22:47:17
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  I have had a ROUX-EN-Y (a form of gastric bypass). I was a Kaiser patient for 20 years or so. They did the operation and a number of other related operations. I think that I could get my records from them. \n\nMy father was an alcoholic and his father was an alcoholic.\nMy mother was diabetic and her mother was also diabetic.\n\nI think that this is related to my compulsions.\n\nIt may not be rare enough for your study, but it has been a serious problem all my life.\n\nMy uncle has traced back my father's  family history for many generations.\nI have a cousin that has traced back some of my ancestry on my mothers side in great depth. < http://wc.rootsweb.ancestry.com/cgi-bin/igm.cgi?op=SRCH&db=pricefrielgrow&surname=P>  My mother and aunts and uncles all had Type 2. My cousin's daughter died of Type 1. \n\nTo quote him: \n"My oldest daughter Amanda was diagnosed with Type 1 diabetes just before her 3rd birthday in 1978.  At the time, I was not aware of any relatives on my side of the family nor her mother's who had juvenile diabetes.  Amanda died just before her 24th birthday.  Since then I have been very alert for anyone else in the family who may have had diabetes.  I later found out that Amanda's maternal grandmother had diabetes, probably Type 2, but she lived to 86.\n\nAmanda suffered from another auto immune disease, interstitial nephritis.  She lost her kidneys at age 11.  In addition she suffered from seizures which were controlled with medication.  Amanda's younger sister and brother have not shown any sign of diabetes.\n\nI learned last year that Teresa Friel Price's older brother Leo Bernard Friel had diabetes, and that his son Emmett William Friel died in 1946 from diabetes at age 27.  I assume this was type 1.\n\nAlso Mary Kathleen Curran, granddaughter of Teresa Price's older brother Emmett Albert Friel, told me that her son Jimmy Sloan contracted type 2 diabetes at age 42.\n\nI am not aware of anyone else in the family who has been diagnosed with diabetes, but it is certainly possible.\n\nMy theory is some people are genetically predisposed to get Type 1 diabetes and that it takes a virus (coxsackie?) or stress to trigger it.  This gene may be in the Friel line.  I have not found anyone in the Price line with diabetes.\n\nI would be interested to know if any of your family has diabetes.\n"\n\n\n


human_id: huFDF88E
date: 2011-07-21 09:34:54
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Severely react gastrointestinally and vascularly to a number of medications and environmental chemicals. Chemically induced cardiac disease.


human_id: huFDF88E
date: 2011-07-21 09:34:54
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  UGT 1A1 under function. Artheriosclerosis. Elevated SOD, GSHPx. Gilbert's syndrome. (Should already be in file.)


human_id: hu35389E
date: 2011-07-23 11:43:57
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  Lab results (T4, parathyroid hormone levels, blood calcium levels)\nSestamibi imaging for hyperactive parathyroid


human_id: huB220C0
date: 2011-07-25 16:00:28
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Autoimmune disorders - Sjogren's, Lichen Scleroderma, Microscopic Colitis (Lymphocytic), Hashimoto's Thyroiditis, Psoriasis (blistering), very high ANA. Juvenile Diabetes runs in the family (uncle, grandmother and cousin). Also have epilepsy. Answers are for Autoimmune disorders in general.


human_id: huFAE9C8
date: 2011-07-25 20:35:18
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  My dad is affected, and his mutation was mapped to 3766 C>T (Q1256X) at Baylor via a clinical genetics test -- I have a copy of that report. Although I haven't formally been sequenced at APC by Baylor (or any other clinical genetics lab), I did recently confirm my mutation by direct sequencing for myself. Which confirms I have the same mutation, consistent with the autosomal dominant inheritance of the disease. We also have plenty of endoscopic images of the polyposis and associated extracolonic manifestations of the disease (Gardner's Syndrome).


human_id: huD09534
date: 2011-07-26 00:18:34
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Endometriosis has not skipped any women in my family for a few generations at least, and for some its been very problematic, even ruining fertility


human_id: hu8471D8
date: 2011-07-26 17:54:34
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have major depressive depression and social anxiety disorder.  My mother suffers from and has been formerly diagnosed with bipolar syndrome.\nI am answering the following questions in regards to major depressive disorder.


human_id: hu8BEAFA
date: 2011-07-26 17:56:49
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I was diagnosed with Malignant Melanoma at the age of 24.  I was told by many physicians that this diagnosis is more common in the 50+ age group and is more than likely a genetic reason to why I was diagnosed with this at such an early age.


human_id: hu94CD59
date: 2011-07-26 18:16:42
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  MTF Transexual. May be due to hormone mix in the womb but could also involve my or my mother's genetics. At this point no one knows.


human_id: hu94CD59
date: 2011-07-26 18:16:42
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  There are no tests for transsexualism that I am aware of but I have transitioned and been treated for over a decade and can provide doctor's names and information release forms.\n\nBy the way, you need more choices for sex than simply male, female, and no response. You should at least add MTF and FTM transsexual as well as choices for various types of intersex, cross-dressers, androgynous, etc.


human_id: hu2DBF2D
date: 2011-07-26 18:30:44
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Two rare traits: Attention Deficit Disorder (lifelong symptoms) and Geographic tongue (began as a teenager and has gradually increased in frequency)


human_id: hu7A114C
date: 2011-07-26 18:48:28
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have a condition called dermatographia, which is also known as the Skin Writing Disease. My body responds with hives directly to any area scratched on the skin. I can write or draw on my body by simply scratching my skin. The skin surface of the area scratched will raise and turn pink. The hived-area takes approximately two minutes to form and remain anywhere from 5 - 45 minutes. The following answers will be in relation to my Skin Writing.\n\nI also have one eye that is physically placed higher on my face than the other. I have to have corrected vision lenses, and they must have prism in them or I will see double. As people with lazy eyes have to have their vision corrected horizontally, due to one eye being higher than the other, I have to have it corrected vertically. Due to this, I am unable to wear contacts, and am currently not a candidate for any sort of laser vision sugery.


human_id: hu8F918A
date: 2011-07-26 19:48:32
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Heart disease/stroke.  Several paternal relatives (father, grandfather, uncle) and maternal grandfather died of heart disease.  While the genetics have not been elucidated this indicates a genetic disease trait.


human_id: huB9F2F3
date: 2011-07-26 19:51:31
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Melanoma cancer.  Mother had it. Maternal uncle died of Melanoma. I have had one removed and my sister has had one removed.  Father had Basel Cell


human_id: huB9F2F3
date: 2011-07-26 19:51:31
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  I can get doctor's reports on myself and my mother on melanoma.  Same doctor removed both of our cancer sites.


human_id: hu3D355A
date: 2011-07-26 22:27:35
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Cholinesterase inhibitor sensitivity: I seem to have unusual degree of problems which seem related to consumption of nightshade foods (potato, tomato, peppers, eggplant, etc.) and possibly pesticide exposure in ways which seem consistent with enhanced sensitivity to cholinesterase inhibitors found in these compounds.  More info at https://sites.google.com/site/annerwright/cholinesterase-inhibitors  I suspect genetic origin for this.  I suspect my mother may have been similarly affected, but she passed away before I had developed this line of inquiry.  I have found several publications, particularly by the Soreq Research Group in Jerusalem, discussing genetic polymorphims consistent with these effects. Also, certain atypical SNP results identified by running 23andme raw data through Promethease may contribute or synergize with these effects.  More info at https://sites.google.com/site/annerwright/snps


human_id: hu75BE2C
date: 2011-07-26 22:45:18
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  PGP Participant Survey (July 2011).\n\nQUESTION: "Do you have a severe disease or rare non-disease trait you believe is strongly genetic in origin? Please describe."\n\nWilliam Hamilton STEWART wrote the following on 2011/Jul/26.\n\n1) SUPER MUSCULAR STRENGTH - I have been four times stronger than most people even though I never had any athletic training, etc..\n\nThe strength of every part of the bodies of college students was tested in the 1960s as part of a national survey for military purposes. One student in my Physical Education class at the University of South Carolina always doubled the test scores of all of the other boys. I always doubled his.\n\nI was one of the last students in my class to be tested via a scale attached to a belt that was strapped around our waists. According to that scale, except for one boy and me, the most each of the approximately forty members of my Physical Education class at USC could lift was about 400 pounds.\n\nI thought I would test the device to see how it felt before I tried very hard. I'll never forget the bulging eyes and expression on the face of USC football coach Lamar as I gently lifted up on that scale. He blurted out: "Stewart, what did you do to that thing?". He always cut my scores in half. I left well enough alone.\n\nWhile my Uncle Joe STEWART and I were sitting at his kitchen table one day, the subject of our family's strength came up. I told him I could lift the back end of my 1958 VW (65% of the total weight of the vehicle). He did not believe me so we walked out into his front yard. His eyes bulged and his mouth flew open when he saw me snatch the rear wheels of my VW completely off the ground  with my bare hands. I stopped lifting my VW after it occurred to me that lifting that much weight might not be good for my spine.\n\nMy brother told me he had similar experiences. He grew several inches taller than me. My parents never abused my two brothers. My brothers and I never smoked or used alcohol and other drugs. My parents bought candy, colas, junk food snacks and toys for them, but never for me.  One of my Stewart cousins told me he was super strong too.\n\nHow much of our strength is genetic? My childhood environment was terrible.  My parents physically and mentally abused me from the time I was a baby until I graduated from High School and left their home. They worked me like a slave and starve me on a diet of grease and grits six days a week. It made me so sick every few weeks that I vomited and could not eat. I usually became well after a few days because my mother put me in bed and fed me some fruit salad. I was hospitalized when I was five or six years old because of a bone infection of a bruise, i.e., osteomyelitis. I spent several years in hospitals because there was no penecillin for the civilian population during World War II.\n\nA doctor who measured my pulse when I was a teenager said it was 39. Until a few years ago my resting heart rate was still 39.\n\n2) FAST RUNNER - I enrolled in a jogging course at USC during the 1980s. For our final grades college students who were half my age and I had to run two miles around a square athletic field. We had to run around that field four and half laps on grass in order to run one mile. We had to slow down 18 times every mile because we were not allowed to cut corners. I ran the first mile in four and a half minutes so the two timers shouted for me to slow down. I paid no attention to them and ran the second mile in four and a half minutes too. I felt that I could run at that speed all day long. I never push myself to the limit because I do not want to risk injuring myself. I and another guy received the only "A" grade in that jogging course.\n\n3) FAST SWIMMER - I won all the swimming and other athletic competitions at the camps (e.g., YMCA) that I attended during summer vacations as a child. I was never trained to do any sport.\n\n4) INTELLIGENCE - The University of SC gave me some intelligence tests about 1960. I do not attribute my IQ score of about 140 to my having a better environment than most people. My mother spent her childhood working in a cotton mill. My alcoholic father could barely read and write.\n\n5) POSSIBLE SENSITIVITY TO ELECTROMAGNETIC FORCES\n* My nerves tingled so badly that I could hardly stand being swung back and forth when I was a child, possibly because my nerves are more sensitive to the earth's magnetic field than other people's.\n* I felt the build up of an electromagnetic charge moments before I was struck by lightning in the 1970s (not strongly enough to kill me fortunately).\n* The first time I attempted to use a cellular telephone it had a destructive effect on my nearby nerves and other tissues.\n\n6) STRONG EMOTIONS - My dog had ten puppies. I love them and want them to be healthy and happy. I have wept because of the suffering and death of three of them. I also love people and science. I want our civilization to continue to survive and make progress.\n\n7) MY ANCESTRY - All of my known maternal and paternal ancestors have lived in SC since the eighteenth century. Many of my cousins have had DNA tests. That all of them belong to Y-haplogroup "R1b1a2" and to haplogroup "I" may mean that I am of almost 100% European, i.e., Celtic and Viking (Germanic) ancestry.\n\nI belong to Y-haplogroup "R1b1a2a1a1b4" (R-L 21, L459) and to the same Stewart family as the kings of Scotland. See FtDNA ID 143035 at http://www.familytreedna.com/public/Stuart/default.aspx?section=yresults ,


human_id: hu56B1F0
date: 2011-07-27 06:38:31
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  For remaining questions I will answer the questions using the genetic diagnosis as the main disease/trait. \n\nPRIMARY DIAGNOSIS/GENETIC:\n46,XX,der(8)t(8;12)(p23.1;p13.31). \nUsing array nomenclature, Jacqui's translocation is described as: arr cgh 8p23.3p23.1(181,530-6,929,747)x1,12p13.3p13.31(100,682-8,123,572)x3. \n\nOTHER TRAITS:\n(1.)Wolff-parkinson-White syndrome with two bypass tracts. (2.)Seizures with status epilepticus. (3.)EXTREME OBESITY SINCE INFANCY (the single most difficult part to deal with). Severely calorie restricted diet since infancy. (4.)Tumor/cyst on pineal gland adjacent to quadrigeminal plate. Not growimng or changing/followed with MRIs (5) Hypotonia. (6.)Hearing impaired (bilateral aids). (7.)Developmentally delayed (approx 55 IQ by testing- performs 10 points higher than tested IQ when not tikmed.) (8.) Hemiparesis. (9.)HARLEQUIN COLOR CHANGE from birth to age 6 months. (10.)Orthopedic involvment of feet (one varus and one valgus defor,ity. Club foot. One foot size 5 1/2 ladies shoe one foor size 9 1/2 shoe. (10.) High arched palate. (11.)narrow short forehead. (12.)Bushy eyebrows. (13.) Teeth=orthodontia and rooots resorbed.(14)TALKITIVE. (15) OCD. perseverates. (16) Happy Angelic temperament. (17.) excellent reader. (18.) Singing- a natural gift of a beautiful soprano singing voice is a strong quality. Only reporting most significant traits. leaving out all other traits for the present. etc.etc...\n\nThis is being reported by mother, Mary Anne Slevin, who is also enrolled in study.(enrolled at jacquianne7@yahoo.com). I have Jacqueline's power of attorney for health care and have communicated in email with Dr.Joseph Thakuria at your department and he should be familiar with this patient.\n


human_id: hu56B1F0
date: 2011-07-27 06:38:31
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  FISH. CGH ARRAY. Methylation study for PWS (negative study).   I cannot upload to your website. I do not have a scanner at the moment and my computer will not permit me to upload. I have emailed attached copies to Dr. Joseph Thakuria at your PGP project so he should already have them for your perusal.\n\nI do not want any personally identifyable information specifically as it relates to patient's personal name, age, doctors names, test laboratories, location of patient's residence, etc. made public. Only confirmed genetic test results (karyotype, phenotype, etc.) are authorized for public dissemination at this time.


human_id: huD2DC60
date: 2011-07-27 07:11:57
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  \nMother to adult daughter with extremely rare genetic rearrangement (see below). \nAlso, \nI have just been diagnosed as pre-diabetic after several high fastimng blood sugars and two different hba1c tests results of 6.2.  Am due to re-test again in November 2011 and will request other diabetes tests at that time. We have a very strong family history of Diabetes. Both types 1 and 2.  \nMy 1st cousin is a doctor at your hospital and knows the family diabetes history. \n\nGENETIC:\nMOTHER OF ENROLLED PARTICIPANT (mnvbn@msn.com)WHO HAS:\nder(8)t(8;12)(p23.1;p13.31). \nUsing array nomenclature, her translocation is described as: arr cgh 8p23.3p23.1(181,530-6,929,747)x1,12p13.3p13.31(100,682-8,123,572)x3. \n\nFOR THE REMAINDER OF THIS SURVEY, since I can only select one disease, I WILL ANSWER QUESTIONS BASED ON THE REPLY OF "DIABETES".\n


human_id: hu42B208
date: 2011-07-27 08:57:10
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  One APOE4 allele, increasing my risk of developing Alzheimer's disease. Two of my grandparents died of Alzheimer's disease.


human_id: hu5A0C00
date: 2011-07-27 09:57:47
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  My grandmother, mother, sister, uncle, and myself all have malformed and missing thumbnails, patellas, various double joints and back problems. I have personally had knee cat scans, a back MRI, and can take pictures of my thumbs. (I have also developed ankylosing spondylitis.


human_id: hu5DB8A1
date: 2011-07-27 14:17:39
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I had severe preeclampsia during my first pregnancy (including a pre-term low birth weight child), and mild preeclampsia during my second pregnancy. I also have a focal dystonia, which may or may not have a genetic predisposition.


human_id: hu5DB8A1
date: 2011-07-27 14:17:39
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  I have copies of all the medical records throughout my pregnancy including lab tests and blood pressure progression, and fetal information prior to and after the birth.


human_id: huFEDA9B
date: 2011-07-27 19:29:03
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Exercise induced hives - I break out in hives from "sprint" or burst style activity\nI also have an indented chest, although I know that is common


human_id: hu23FAE3
date: 2011-07-28 20:10:28
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  Laboratory request was made by Dr Bill Nam Wong, MD, lung specialist, Valley Care Hospital, Pleasanton, CA, to an outside laboratory to test for mutations of clotting factors during an episode of pulmonary emboli. \nA request can be made to the laboratory if PGP requires a report directly uploaded from the testing laboratory.


human_id: hu8DD372
date: 2011-07-29 23:27:44
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  Complete medical history, including:\n*Standardized neuropsychiatric evaluations\n*Comprehensive blood panels\n*MRI imagery


human_id: huD6D3D9
date: 2011-07-30 00:19:31
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have bi-polar disorder, which is being successfully managed with medication for about the last 20 years. Alcoholism runs in my family, with alcoholics in both maternal and paternal lines. Some of my siblings self medicate; my sister is married to an alcoholic.


human_id: hu2FEC01
date: 2011-09-03 11:55:12
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Absolute pitch,\nAsperger's syndrome,\nColorblindness (mild red-green),\nHomosexuality [described hereafter]\n


human_id: hu01A67D
date: 2011-09-04 17:25:31
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I'm an INTJ personality, which according to Kiersey is less than 1% of the population.  Further, I match better with Kiersey's definition of it ("Mastermind") than some others that use "scientist".  Think Spock.


human_id: huF5AD12
date: 2011-09-16 19:33:32
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Very Superior IQ (WAIS-IV FSIQ 145 99.9 Percentile, VCI 150 >99.9 Percentile)\nBipolar Disorder\nADHD\nMigraine\nHomosexual\n


human_id: huF5AD12
date: 2011-09-16 19:33:32
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  WAIS IV testing results for IQ.\nAs for the others, ADHD, migraine, and bipolar have all been formally diagnosed, and I am happy to share my records. I have the autistic tendency towards full disclosure to an extent that sometimes violates social norms or other's comfort level; I really don't have any problem with anyone knowing the details of me being a crazy gay smart guy to the limits of their voyeurism. I wasn't going to bother putting everything into Google Health since it's being discontinued, but since you're going to keep the data alive I might as well. That's going to take a few weeks, as I have hundred of pages of medical records already and probably a few hundred more on the way. Happy, happy, joy, joy.


human_id: hu5917F3
date: 2011-09-17 13:10:14
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have multiple sclerosis, which previous research has indicated to have a significant genetic component.


human_id: hu5917F3
date: 2011-09-17 13:10:14
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  There is no genetic test for multiple sclerosis.  Diagnosis is based on clinical symptoms and confirmed by MRI and lumbar puncture showing oligoclonal bands in the spinal fluid.  I have had several MRIs showing characteristic signs and had a spinal fluid electrophoresis showing oligoclonal bands.  These tests were done by a neurologist at Kaiser Permanente in Los Angeles and I believe I could request copies of them if that would be of interest, although I have not yet done so.\n


human_id: hu9002DE
date: 2011-09-20 19:32:20
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Ability to perceive relationships among events, phenomena, people etc. which others see as disconnected.\n\nAbilty to  think objectively & quantitatively about all phenomena, reguardless of emotogenic connotations.


human_id: huA0E089
date: 2011-09-26 15:56:25
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have been diagnosed by genetic testing to have FSHMD or fascio scapulo\nhumeral muscular dystrophy


human_id: hu23FAE3
date: 2011-09-27 19:54:54
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  The laboratory of the hospital in Pleasanton, CA, sent out my blood sample for genetic testing. I can request that the results be sent to PGP.


human_id: hu0352A7
date: 2011-09-30 17:20:14
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have gender identity disorder.  I am biolgoically female, but inject testosterone and have gotten a double mastectomy.


human_id: hu8BEAFA
date: 2011-10-10 11:47:54
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I was diagnosed with Malignant Melanoma at the age of 24, which to my understanding is the average diagnosed age is 59, and there is only 8% of people diagnosed in the U.S. that are between the ages of 20-34.  So I feel that there is some sort of genetic disposition that I have that could have been a player in my melanoma diagnosis.


human_id: hu337BB4
date: 2011-10-12 10:58:45
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Psoriasis. Not seen on my Father's side. Mother was adopted, so her side of the tree is unknown to me.


human_id: hu6D1115
date: 2011-10-16 00:51:42
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have high homocysteine although I control it with Folgard 2.2 rx\n\nI don't know if this condition is considered *rare* but mine is definitely genetic in origin as my father also had the condition. I suspect that my paternal grandmother and uncle also had it.


human_id: hu6D1115
date: 2011-10-16 00:51:42
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  I saw a pediatric geneticist at UCLA (Ronald Reagan Medical Center) who had me tested for a couple of gene variants and other factors. I have the test results as well as his narrative. However, I do believe there are also other gene variants relative to this condition that I haven't been tested for, such as MTHFD1L. I'm very curious about my risk for Alzheimer's as it relates to homocystememia. I am homozygous for APOE 3 and no one in my family has developed dementia BUT on my father's side where the homocystemia comes from, they tended to die of cardiovascular disease/stroke before late onset dementia could present.


human_id: hu52B7E5
date: 2011-10-21 18:36:58
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I was diagnosed with invasive lobular breast cancer at age 39.  My mother was diagnosed with breast cancer at age 43, my aunt at age 48, and my maternal great-grandmother at 43.  The four of us represent 50% of the women in our four generations.  I was tested for the BRCA 1 and 2 mutations and the CDH1 mutation and did not have any of them.


human_id: huAA245C
date: 2011-10-21 20:48:00
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  I have many films for my dextrocardia that I would be happy to send via mail but none that I am able to upload. The films are from many years ago.\n\nMy craniopharyngioma was documented via multiple MRIs and frozen section histology studies during the removal surgery.


human_id: hu47B0B2
date: 2011-10-23 06:22:18
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Waardenburg Syndrome - my symptoms are deafness in left ear, pre-mature grey hair and wide set eyes. \n\nFrom Pub Med Health:\nhttp://www.ncbi.nlm.nih.gov/pubmedhealth/PMH0002401/\n\nWaardenburg syndrome\n\nKlein-Waardenburg syndrome; Waardenburg-Shah syndrome\nLast reviewed: August 4, 2011.\n\nWaardenburg syndrome is a group of conditions passed down through families that involve deafness and pale skin, hair, and eye color.\n\nCauses, incidence, and risk factors\n\nWaardenburg syndrome is inherited as an autosomal dominant trait, meaning only one parent has to pass on the faulty gene for a child to be affected.\n\nThere are four main types of Waardenburg syndrome. The most common are Type I and Type II.\n\nType III (Klein-Waardenburg syndrome) and type IV (Waardenburg-Shah syndrome) are more rare.\n\nThe multiple types of this syndrome result from defects in different genes. Most people with this disease have a parent with the disease, but the symptoms in the parent can be quite different from those in the child.\n\nSymptoms\n\nSymptoms may include:\n\nCleft lip (rare)\n\nConstipation\n\nDeafness(more common in type II disease)\n\nExtremely pale blue eyes or eye colors that don't match (heterochromia)\n\nPale color skin, hair, and eyes (partial albinism)\n\nDifficulty completely straightening joints\n\nPossible slight decrease in intellectual function\n\nWide-set eyes (in Type I)\n\nWhite patch of hair or early graying of the hair\n\nLess common types of this disease may cause problems with the arms or intestines.\n\nSigns and tests\n\nTests may include:\n\nAudiometry\n\nBowel transit time\n\nColon biopsy\n\nGenetic testing\n\nTreatment\n\nThere is no specific treatment. Symptoms will be treated as appropriate. Special diets and medicines to keep the bowel moving are prescribed to those patients who have constipation.\n\nExpectations (prognosis)\n\nOnce hearing problems are corrected, most people with this syndrome should be able to lead a normal life. Those with rarer forms of the syndrome may have other complications.\n\nComplications\n\nConstipation severe enough to require part of large bowel to be removed\n\nHearing loss\n\nSelf-esteem problems, or other problems related to appearance\n\nSlight decreased intellectual functioning (possible, unusual)\n\nSlight increased risk for muscle tumor called rhabdomyosarcoma\n


human_id: hu098181
date: 2011-10-25 15:41:56
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Lactose intolerance (discussed in detail below [my uncle is also lactose intolerance but this project has not been discussed with him])\nI am 100% Jewish, there is a chance I am a carrier of Tay-Sachs (my mom, dad, brother and potentially all of my grandparents are interested in participating in the PGP, at least one of which has already enrolled)


human_id: hu098181
date: 2011-10-26 16:21:54
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  I have test results from two bronchial infections that resulted in an outbreak of asthma that has lasted me for nearly 20 years now, as well as the medications provided, etc...


human_id: huDA2757
date: 2011-10-26 23:34:01
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Multiple:\n\nMy IQ consistently tests over 160, and typically in the 170-180's, for spatial skills and mathematic comprehension.  Verbal ability is within the high end of "normal".  Numerous family members have been above average at math, science, and spatial reasoning.\n\nI also have "ventricular branch delay" as described by a cardiologist.  I have relevant medical data and testing information for this, but from my understanding of these tests, the most obvious result is that in my ECG, part of my R wave fires during my S wave creating a "jaggie" in the S wave.  From what I understand, this is a rare, but trivial, electrical defect in the heart, though a cardiologist would have to comment on this further.  There is a strong history of heart related illness in my family, so it is very possible this is genetically linked.\n\nI have recently been diagnosed with migraines, which apparently affects <1% of adult males, and there is a strong history of headaches on my mother's side of the family.\n\nI was tested at age 18 to have 115% of normal tidal volume for my external body measurements, and have been able to achieve a *standing* heart rate of 40 beats per minute due to exercise alone.  My father's side of the family have typically been endurance athletes in their early years, and most of us have ectomorph body types.\n\nFinally, I appear to have inherited chronically low testosterone levels from my father, who also suffers from this condition.


human_id: huDA2757
date: 2011-10-26 23:34:01
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  Mensa test results for IQ.\n\nFor heart information, all medical information should still be on file at the cardiologist's office to include NMRI, holter moniter data, echocardiogram video, stress test and EKG.  However, I do have the EKG printouts and the doctors written notes.\n\nHeart rate would also come from cardiologist's information, and tidal volume data should be the same if tested now.\n\nTestosterone levels can be verified through recent blood tests.


human_id: huD554DB
date: 2011-11-01 15:38:29
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  seizure disorder that might be mitochondrial based, son with significant clinical features of mitochondrial disease, I have had numerous rare reactions to a variety of types of medications including life threatening reactions


human_id: hu0A8345
date: 2011-11-07 01:12:50
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  Paper Summary of Test Results\nMR Brachial Plexus\nMR Brain - With and Without Contrast\nMR Cervical Spine - Without Contrast \nMR Lumbar Spine - Without Contrast \n\n\t\n


human_id: hu7F99E2
date: 2011-11-09 08:55:33
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have had severe asthma since I was 8 years old. My father outgrew his when he was an adult but myself at 34 years old still has it. I also was diagnosed with Ankylosing Spondylitis (spinal arthritis on my spine- joints and my spine is fusing) 3 years ago and also have degenerative disc disease (my discs are herniating and, dehydrated) in my spine.\n\nMy biological mother was just diagnosed with Rheumatoid Arthritis and my bother has bone spurs and disc issues as well. I believe these are all hereditary. I have extremely high ANA titers as well when blood is taken and I am HLA-B27 positive.


human_id: huFAF983
date: 2011-11-15 10:39:38
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have Fuch's dystrophy- causes deterioration in the lens leading to blindness. My mother suffers from this also.


human_id: huFAF983
date: 2011-11-15 10:39:38
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  I could upload the statement of my Optthamologist at a minimum. I could determine if sone oof the images could be photographed and then sent to me.


human_id: hu6426D7
date: 2011-11-16 16:51:46
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  My family is riddles with mental health issues--severe anxiety, PTSD, psychopathic behavior and addiction, and autistic traits.  Thyroid issues also common.  One child presented multiple birth defects.


human_id: huD554DB
date: 2011-11-23 11:58:13
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  son suspected in having a mitochondrial disorder with numerous chronic health issues typical for mito, I developed adult onset seizures with no known cause, with numerous rare reactions to medications such as phenobarbital and tegretol, half sister having EEG today for adult onset seizures similar age to my onset


human_id: huD554DB
date: 2011-11-23 11:58:13
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  EEG results, some DNA analysis completed related to mito with a trait identified in both son and self that may or may not be indicative of an issue


human_id: huCD380F
date: 2011-11-23 12:17:40
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Balanced translocation on chromosome 18, which resulted in child born with monosomy 18p (microdeletion).


human_id: hu3B94BD
date: 2011-11-23 13:01:55
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Rare trait -- a profound impairment in episodic memory despite being in top 1% on IQ, having above average working memory, and superior semantic memory for book learning and technical data. Often after a few years I will have a complete absence of recall of having gone on a vacation, no recollection of having visited a country or met up with friends, and can't recall even after seeing photographs with myself in them or being told of the trip. Also significant visual prosopagnosia, e.g. difficulty recognizing my father in crowded train station. No history of trauma or brain injury.


human_id: hu259AC7
date: 2011-11-23 14:23:22
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Kallmann Syndrome/Hypogonadotropic Hypogonadism (used for the following questions)\n\nI also have Human Growth Hormone Deficiency and Asperger's Syndrome.\n\nI was born with all of these conditions.


human_id: hu259AC7
date: 2011-11-23 14:23:22
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  I have had numerous blood tests, monitoring testosterone levels and such.  The results of the majority of these tests would be in the possession of Dr. Edward Reiter, who was my Pediatric Endocrinologist.  He is/was based out of Springfield, Massachusetts.


human_id: hu6D1115
date: 2011-11-24 03:10:23
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  It is not that rare, but potentially severe. I'm hetrozygous for MTHFR C677T. When I was diagnosed in 1998, my homocysteine level was 48. That is pretty high for a CT. There have to be multiple factors at work to drive my homocysteine level so high. It isn't my diet as I'm a healthy eater. What could they be? Recently I came across a study that sheds some light on my question. I found out that in combination with MTFHR 677>CT, I am a homozygous CC for SLC19A1 rs819130 which supposedly causes a 10% increase of homocysteine levels in carriers on top of whatever effect the MTHFR>CT has. rs819130 is a folate transporter, but in CCs, not efficient. As far as I can tell, no one quite has a handle on high homocysteine yet. I follow the research avidly hoping to find out as much as I can about my condition, so I can figure out how to moderate my epigenome to counteract the effects. I've seen what it did to my father, my uncle and my grandmother. I'm aware of what it did to my great-grandmother. None of them lived long enough to be affected by late onset Alzheimer's but high homocysteine is a risk factor. Alzheimer's is definitely a fate I wish to avoid. So far I think my best bet is strenuous daily exercise and reducing my calorie and sugar intake. I also have risk factors for diabetes, so I've been trying to eat like a diabetic as best I can.\nAll the people in my family who share the high homocysteine trait are now deceased, so they won't be enrolling in PGP. My brother has a rare neurological disease. MSA (symptoms similar to ALS). He is enrolled in a trial through UCLA, but he's getting worse, and they think he's probably getting the placebo. His wife is planning to take hin to China for a stem cell transplant. However, I doubt that his issue is related to mine. I wouldn't dare ask him to enroll in PGP at this point.\n


human_id: hu6D1115
date: 2011-11-24 03:10:23
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  I have genetic tests from Berkeley Heart Lab and Health Diagnostic Laboratory that confirm MTFHR 677>CT. I have a subscription to 23and me that allows me to browse raw date, so I'm able to correlate my condition to the latest genetic research on high homocysteine. I was first tipped off to my condition after my father had a heart attack in Canada. His cardiologist told him he had the highest level of homocysteine that had ever been tested in the lab that covers all of Western Canada and that his condition was genetic and all his children should be test for it. None of my sisters have it. I'm not sure about my brother, but I don't think he does either. Classic one out of four.


human_id: hu9002DE
date: 2011-11-28 14:01:16
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Ability to perceive relationships among, & implications of, data that others rarely seem to perceive. \n\nCognitive objectivity.


human_id: huD554DB
date: 2011-11-28 19:46:46
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Son and I have novel homoplasmic mutation formally designated as 14751C>T leading to an amino acid change from threonine to isoleucine\n\nI have also had rare life threatening reactions to tegretol and phenobarbital, adult onset seizures unknown origin


human_id: hu3EFFEE
date: 2011-11-28 21:49:45
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  I think that I have test result desriptions (no images) of biopsies, iodine uptake tests, etc.   After they removed the thyroid they found a small malignancy on it and I might have those results as well.  I don't have all of my tests since they go back over 30 years, but I'm sure I have blood tests and some scan results.


human_id: hu432EB5
date: 2011-12-07 02:16:39
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Von Willebrands disease type 2N (considered rarest).  Idiopathic adult onset growth hormone deficiency.  Idiopathic syringomyelia.


human_id: hu432EB5
date: 2011-12-07 02:16:39
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  I have the results of the gene mutation test for VWD type 2N, as well as numerous von-willebrand factor and factor VIII activity lab results.


human_id: hu9002DE
date: 2011-12-24 20:51:51
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Probable Genetic Vascular Defect: My biological mother died at age 55 from a burst berry aneurysm of the Circle of Willis. As a child she hasuffered so much from what is commonly called "prickly heat" that she had to drop out of hi school for a year.  I sometimes had prickly heat on my chest as a child, but never so severely that it changed my life activities.  At birth I had 2 strawberry birthmarks - one just below my left clavicle, and a larger one, about 2" x1" in size, located 1" to the left of my lumbar vertebrae. They were burned off with Radium when I was a baby. At age 30 a cavernous hemangioma was found in the upper frontal bone of my skull. It was removed & replaced by a plastic plate. A CAT scan at age 60 reported no signs of brain aneurysms.


human_id: hu48C4EB
date: 2011-12-28 15:55:52
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have Rheumatoid arthritis since the age of 13.  I know that my cousin has had it since birth, and a great uncle had it as well. (all on my mothers side)\n\nI also have wide hips (for a man) that I believe is a combination of my Dad's broadly built frame and my Mother's more average frame.


human_id: hu9F7183
date: 2012-01-18 10:32:18
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have fairly mild eosinophilic fasciitis, and mild asthma/allergies. My sister has MS, my brother had some severe ulcerative colitis leading to large bowel removal, and my mother died (at 84) with some idiopathic pulmonary infiltrative disease. I would suspect some inherited tendency to autoimmune/inflammatory processes that may present in different organ systems and which may not be recognized in a single disease entity.


human_id: hu9F7183
date: 2012-01-18 10:32:18
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  I do not have all data in hand immediately. But I have access to data from multiple CBC/diff studies (documenting eosinophil counts most relevantly), serum albumin, assays for ANA, etc., widely sued for autoimmune disease assessments.


human_id: huD67BC6
date: 2012-01-20 04:09:23
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Three: unilateral deafness (father and grandfather also had, and grandfather's sister was completely deaf), Thalyssemia minor, and gay


human_id: hu6426D7
date: 2012-01-21 14:18:17
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Family has terrible mental health, hoarding, autism, OCD, and addiction issues.  I'm afflicted by several of these.


human_id: huB921C5
date: 2012-01-25 16:23:43
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Rare tumor, pleomorphic adenoma, right side, head/neck tumor; now, removed. Surgery undertaken in custom program designed in Germany, as US based solutions would have led to partial and permanent facial paralysis.


human_id: huB921C5
date: 2012-01-25 16:23:43
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  This would need to be organised, as the record exists across US, German, and Swiss health domains. Will review and update.


human_id: hu9A0F06
date: 2012-01-29 22:03:05
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Anomalous Aortic Origin of the Right Coronary Artery With an Interarterial Course and Klinefelter Syndrome.


human_id: hu1187FF
date: 2012-01-30 12:41:57
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Homozygous for unfavorable variation in MCR4 gene and FTO gene; severe childhood obesity and insulin resistance\n\nSevere high frequency sensorineural hearing loss, onset in 5th decade of life


human_id: huB9F2F3
date: 2012-02-01 08:02:17
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Melanoma - Mother has it, Sister, Maternal Uncle  all had Melanoma confirmed and removed.  Maternal Uncle died from Melanoma


human_id: huB9F2F3
date: 2012-02-01 08:02:17
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  I have doctor's reports for the removal of the melanoma.  I believe that there are lab tests in those records.


human_id: huD2ECE0
date: 2012-02-03 21:29:28
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have absolute pitch (as highlighted in that survey), but the rare trait I wish to be tracked here is that I have been diagnosed with familial hypercholesterolemia. I am a lifelong vegetarian, and vegan with a predominantly whole plant foods diet for the past 8 years--yet have had cholesterol levels of 255 to 294 over that same period. This trait did not become evident until I reached my forties (diagnosed at 41).


human_id: huD2ECE0
date: 2012-02-03 21:29:28
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  Highest lab test for total cholesterol was 294 mg/dL while vegetarian, in excellent athletic shape, but not taking statins. I have opted to trust dietary and fitness approaches that lower inflammation--rather than managing my high cholesterol values with statin drugs.


human_id: hu704A85
date: 2012-02-05 00:23:30
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Sometype of muscular dystrophy and heart problem, possibly related,  I have had a muscle biopsy but they could not define my muscle disease.


human_id: hu704A85
date: 2012-02-05 00:23:30
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  I have muscle biopsy results and results of test on my heart.  The MDA clinic did some genetic testing but It was negative for duchane and others they tested for.  They do not know what is inflaming my muscles and causing them to not regenerate.  I believe my mother died from what ever this is, so\nI am very interested in your study.


human_id: hu1B30FD
date: 2012-02-05 13:29:42
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  FAA has documentation that says I fail the standard color vision book, but pass the control tower red, green, white test. My first born sibling, a male now 82, is not color defective; my late younger brother was color defective; my sister, last born, is not color defective.


human_id: hu9F027E
date: 2012-02-14 23:12:05
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Atrial septal defect (ASD).  Repaired at age 6.  My son has an unusual murmur and my daughter was born with tetralogy of Fallot (repaired 6 mos).  We provided some saliva for a study at Mt. Sinai Hospital in NY in 2006, but not certain if that lead to anything.\n\nAlso, anxiety/depression


human_id: hu9F027E
date: 2012-02-14 23:12:05
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  Provided I could retrieve it from my physician I could provide ECG and cardiac ECHO data (and whatever else I can get) for myself, my daughter and my son.


human_id: huD95DAB
date: 2012-02-28 22:59:24
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have medium range RA. Seeing Rheum in Dallas and taking all the appropriate drugs.  I have high blood pressuse with meds and high colesterol and triglycerides with meds.  I'm depressed from all the pain - on meds and can't sleep - on meds - I have chest pains and take nitro pills.  But I bets that's as much as you want to hear at this stage.


human_id: huD95DAB
date: 2012-02-28 22:59:24
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  Mostly bloodtest results and xrays from my rheumatologist, Dr. John Willis, next to Baylor hospital.


human_id: hu5FA322
date: 2012-03-04 15:06:10
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  atypical porphyria (affects all systems - used for the rest of questions)\nmitochondria deletions/ROS/frail inner membranes\naortic aneurysms\ndouble null - GST\npoor metabolizer - CYP2C19\nNAT2 - catalytically inefficient\ncancer - prostrate/uterine


human_id: hu254EA5
date: 2012-03-08 19:29:11
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Multiple cysts on kidneys (8-10 each), but probably not Polycystic Kidney Disease (initial diagnosis).  Cysts likely benign.


human_id: hu02BC41
date: 2012-03-18 13:54:21
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Irritable Bowel Syndrome, resulting in numerous traits. These include sporadic bouts of extreme pain in abdomen, rapid weight loss, and severe gastroesophagial acid reflux. The symptoms often are severe enough to interfere with daily life, and seem like an amplification of more mild digestive symptoms that are present in both my maternal and paternal families.


human_id: hu00D419
date: 2012-03-18 16:18:13
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Autoimmune connective tissue disease (SLE and or other connective tissue disease) Age of onset is unknown. Serious symptoms began appearing in 1985. Autoimmunity was not discovered until 2008. The disease is uncommon enough that no one seems capable of properly identifying it.


human_id: huE5A9A3
date: 2012-03-18 16:22:55
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  1) Protein S deficiency (clotting disorder), described below.\n2) Hip deformity.\n3) Hypercholesteremia.


human_id: huE5A9A3
date: 2012-03-18 16:22:55
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  PROTEIN S %\t37\nReference range: 50 to 140\nUnit: %\n(NOTE)\nTest performed at Warde Medical Laboratory,\nAnn Arbor, MI 48108


human_id: huC36EA0
date: 2012-03-20 13:23:57
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  early onset of menopause (both mother and maternal grandmother had early menopause and my fertility issues indicate that I am on the same path). I became aware of this at the age of 39 so that is how I answered below.\n\nbtw - I have been tested for Fragile X and I am not a carrier.


human_id: hu1C50C6
date: 2012-03-21 17:30:20
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  Medical records/images relating to eye exams and surgeries, dental records/xrays (flat facial profile/lower jaw teeth crowding/high soft palate are all associated with Stickler), xrays/medical records relating to arthritis & connective tissue in joints.


human_id: hu254EA5
date: 2012-03-22 22:09:56
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have a large number of cysts on both kidneys. Diagnosed initially as Polycystic Kidney Disease. May be benign.


human_id: huFDF88E
date: 2012-03-24 22:31:58
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have severe reactions to several prescription drugs and diesel exhaust. Testing done by Genova Diagnostics has identified polymorphism at P450 CYP 1B1; CYP 2C19; COMT V158M and NAT2 R197Q. Muscular pain, arrhythmia, vascular pain, gastric distress, respiratory congestion, clotting and illness associated with disorder. Diesel Exhaust sensitivity first identified age 43.


human_id: hu79F922
date: 2012-03-25 14:40:34
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Both parents possessed one mutated (nonfunctional) copy of the SMN1 gene. It's possible that I inherited one of these, but I have not had my genetic material tested yet, so I do not know.


human_id: huBC410F
date: 2012-04-04 16:25:35
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Von Willebrands Disease. (will answer based on that)\nAlso have: Severe scoliosis (greater than 50 degrees). Born with a VSD (hole in heart). Syringomyelia / syrinx.  Asthma. Allergies. Possible Hashimotos (still waiting for test). \n\nStrong family history for depression, addiction, and various cancers including--osteosarcoma, leukemia, breast cancer, lung cancer (nonsmoker), and a pancoast tumor.


human_id: huBC410F
date: 2012-04-04 16:25:35
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  I have PTT results and other bloodwork confirming platelet dysfunction from 2000 through the current year, including surgical records for a spinal fusion where it was tested in response to medication.\n\nI also have copies of medical records for other disorders (MRI scans for syrinx and scoliosis, bloodwork, a tilt test for fainting due to heart problem).


human_id: hu9B93D0
date: 2012-04-04 17:46:19
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  1: I have been very thin my entire life, regardless of the quantity or type of food of I eat.  For most of my teens and twenties I weighed between 120-130 pounds (I am just under six feet tall).  I can eat pounds of chocolate and gain no weight or eat very little and lose no weight.  I only lose weight when ill.  In my 30s (age 31 now) my weight has generally been 125-135 pounds. I have answered the remaining questions in this section specifically regarding this item.\n\n2: I also have rotoscoliosis at T4-T5-T6.\n\n3: I also naturally have very low vitamin D levels.


human_id: hu3A1737
date: 2012-04-04 21:20:26
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Chosen disease/trait:\n\nMultiple neoplasms including lobular breast cancer, ovarian cysts, oral polyps, multiple lipomas..  All neoplasms occured solely on left side of body.\n\nRestless Leg Syndrome\n\nMigraine headaches\n\nFamilial Cholycystitis\n\nBi-polar II\n\nDepression\n\nAdie's/Tonic pupil\n\nAutoimmune process diagnosed as Fibomyalgia\n\n


human_id: huDD3FEE
date: 2012-04-05 09:51:10
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Kleine-Levin Syndrome (decreasing in severity with monitoring and medication per 'Disease/trait: Severity')


human_id: huB441EF
date: 2012-04-05 18:10:01
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Supraventricular Tachycardia - Cardiologist explained that SVT was caused by an extra electrical pathway in the heart and that it is a genetic trait.


human_id: hu3C0611
date: 2012-04-06 05:20:14
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  I have test results from emg.  Results from Neurologist of  blood testing  showing a   deletion of chromosome 17p11.2 ( PMP22g).


human_id: hu7C7FD3
date: 2012-04-09 18:48:03
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I had an idiopathic ventricular fibrillation sudden cardiac arrest, with normal coronary arteries, no cardiomyopathy, normal cardiac MRI scan (ie no arrhythmogenic right ventricular dysplasia), and normal QTc interval, indicative of a probable ion channel mutation.


human_id: hu661AD0
date: 2012-04-16 13:23:32
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have shovel shaped incisor teeth. This is presumably a trait that indicates I have Native American ancestry in the EDAR gene [1]. My mother claims that I have a Native American ancestor (Taino) 3-4 generations ago. I was born a raised in Puerto Rico, and can trace my ancestry back on the island for 8 generations. I think it would be very interesting to find out if I have this variant, and other variants in my genome that are specific to Taino acestry [2]\n\n1: Kimura R, Yamaguchi T, Takeda M, Kondo O, Toma T, Haneji K, Hanihara T,\nMatsukusa H, Kawamura S, Maki K, Osawa M, Ishida H, Oota H. A common variation in\nEDAR is a genetic determinant of shovel-shaped incisors. Am J Hum Genet. 2009\nOct;85(4):528-35. PubMed PMID: 19804850; PubMed Central PMCID: PMC2756549.\n\n2. http://www.nature.com/news/2011/111014/full/news.2011.592.html


human_id: huCBDC6D
date: 2012-04-22 13:09:08
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I am an alcoholic (recovered) from a strongly alcoholic family. All my first degree relatives are or were alcoholics, with the possible exception of my mother.\n\nI am of Irish descent on both sides, and German descent on my father's mother's side.\n\nWhen I drink, I experience severe hangovers, which can last over 24 hours.\n\nWhen I was an active drinker, I would drink very fast and be ahead of my companions, in terms of number of drinks, very early in the evening. Even when drinking alone, I would exhibit the same pattern.\n\nMy hypothesis is this: \n\nI am probably deficient in one of the enzymes that convert acetaldehyde (ACL) to CO2 and H2O. \n\nAs the ACL builds up in my system, rather than experiencing the flushing reaction some people have, I just feel restless and uncomfortable, symptoms which another drink will mask. The result is a very heavy dose of alcohol in a short time, and a build up of ACL to virtual toxic levels, which my body then takes around 24 hours to clear, resulting in a severe, interminable hangover.\n\nAlthough I cannot provide references,, I have read of other people who exhibit this pattern of drinking and this severity of hangover, and have read that it is related to an ACL enzyme deficiency common among Irish people.\n\n


human_id: hu9C27F6
date: 2012-04-23 01:52:55
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  At age 52, I was diagnosed with a defective aortic valve leading to severe regurgitation. There was no indication prior to this and no known illness that proceeded the diagnosis.


human_id: hu52F345
date: 2012-04-25 11:09:37
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I am extremely flexible and can do moderate contortion and have been very bendy since I was a child. I was told by a physician that I have unusually flexible joints.


human_id: huB9F2F3
date: 2012-05-02 06:31:51
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Melanoma Cancer - Maternal uncle died of it, My mother has had melanoma removed as have I and my sister. My father has basel cell carcenoma


human_id: huB9F2F3
date: 2012-05-02 06:31:51
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  I have the lab reports from the dermatologist confirming the cancet. I would have to find it as it was in 1992


human_id: hu3A1737
date: 2012-05-03 15:44:37
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  Lobular Breast Cancer Diagnosis\nDiagnostic imaging films, biopsy and surgical records, surgical sequelae, including repeated hospitalizations for post-surgical MERSA infection,post-surgical treatment plan, current follow-up plan including quarterly lab results


human_id: hu26E291
date: 2012-05-12 06:08:02
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Tarlov's cysts at S1S2 causing pain, neuropathy, bowel and bladder dysfunction.  Treated at John's Hopkins.  Multiple left sided spinal cysts.\n\nMicrognathia needing sagittal spit osteotomy


human_id: hu91F322
date: 2012-05-12 08:53:10
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Diagnosed with enteric reactive arthritis which is associated with HLA-B27 which I had a blood test for and I was HLA-B27 positive.


human_id: hu91F322
date: 2012-05-12 08:53:10
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  I can upload blood test results; there is one showing I am HLA-B27 positive and a lot of them just showing elevated ESR and CRP but nothing else unusual (negative tests for things related to other autoimmune diseases)


human_id: huD3A569
date: 2012-05-24 00:36:19
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  my mother who is 72 has had over 20 skin cancers, basal cell carcinoma and squamous cell carinomas, on her head and face. I have already had one basal cell carinoma on my ear and one squamous on my scalp. Although these are common skin cancers to get, it is rare for an individual to have so many as my mother, and I suspect given that I have had two before the age of 50 that I will have similar problems.


human_id: hu1843FC
date: 2012-05-24 01:00:16
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have tested positive as a Tay Sachs carrier, as has a cousin on my father's side of the family.  My mother is not a carrier per her testing, which means my father is, though he hasn't been tested.\n\nI also have recently been diagnosed with multiple sclerosis, though I do not have typical symptoms.  I initially had a brain MRI due to some cognitive issues I was having which I thought were due to migraines, and this showed lesions which was followed by a spinal tap that showed 9 protein bands confirming a differential diagnosis of MS.  However, I do not have the typical early symptoms.  I believe whatever I do have is genetic in nature because my mother was also diagnosed with MS around the same age. Her symptoms were more compelling in that she had visual issues as well as white matter brain lesions similar to mine, but she only had 3 protein bands.  She, too, had cognitive impairment but never took meds and was later told that she had a single incident rather than the disease.  However, when I took her records to my MS doctor, a leading doctor in the field, he said that she would now still be considered to have MS due to the current criteria.


human_id: hu1843FC
date: 2012-05-24 01:00:16
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  I believe that I could access the genetic testing that I had done that verifies I am a tay sachs carrier.  \n\nMy multiple choice answers pertained to this trait, though I could also download info about the MS and may have a relative willing to participate who was also diagnosed.  I don't have genetic info on the MS, only MRIs and spinal tap results as well as clinical observation notes.


human_id: huC53122
date: 2012-05-28 16:54:43
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I was born with white eyelashes on one eye and brown on the other. Also was born with a large white streak in my brown hair. I was told this was genetic.


human_id: hu9CDD0F
date: 2012-06-09 11:17:07
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have heart disease and it started very early. I do not smoke, and have never smoked. I am overweight, but that is the only risk factor that I have for heart disease. Everyone on both sides of my family suffers from high blood pressure, so my thought is that it must be genetic. \n\nHowever, I'm not sure that it really counts as a severe disease. It may be a leading cause of death, but other than having to have a stent and taking lots of drugs and being careful with what I eat, it doesn't really have much effect on my life. \n\n\nAnother thing, which I've recently learned can have genetic origins is anxiety. Every woman in my family suffers extreme anxiety. Panic attacks, etc. My sister is even on Disability because her anxiety is so severe.


human_id: hu3F8570
date: 2012-06-13 18:00:08
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have been living with Chronic Fatigue Syndrome for nearly 24 years now.  I believe there is a genetic susceptibility to CFS and I'm hoping you can find something in my DNA that might point towards a cause and a cure.


human_id: hu3F8570
date: 2012-06-13 18:00:08
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  Since there is no known cause for Chronic Fatigue Syndrome there is no test for it.  Basically, I've had tests to rule out other diseases with the same symptoms.


human_id: hu5917F3
date: 2012-06-15 20:43:58
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  CSF with oligoclonal bands\nBrain and spinal cord MRIs with and without gadolinium enhancement\nEvoked Potential testing\n


human_id: hu8602F1
date: 2012-06-16 22:43:15
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  I have photographs of my hands, my doctor has tested me extensively for autoimmune disorders with negative results.  My mother had severe raynauds from appx. age 30 until her death at 69. The onset of raynauds in my case was late, October 2011.


human_id: hu11603C
date: 2012-06-22 23:00:36
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Early-Onset Parkinson's Disease (Answering for this disease)\nEhlers-Danlos Syndrome\nBenign Hyperphenylalaninemia


human_id: hu11603C
date: 2012-06-22 23:00:36
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  I have genetic tests that show I have the highest risk for Early-Onset Parkinson's Disease on multiple genes. I also have passed a drug trial to control my symptoms and have been formally diagnosed by a neurologist as having Early Onset Parkinson's Disease.


human_id: hu094BE5
date: 2012-06-23 16:15:35
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have what I believe to be an autoimmune subsystem which is characterized by false chill episodes and a "jumping" or "migrating" deep false itch episodes.


human_id: hu893618
date: 2012-06-25 03:12:00
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  my father and his sister have Alzheimer's.\n\nmy hands tremble which I am told is called benign tremor


human_id: hu9EA336
date: 2012-06-27 18:41:39
phenotype_category: Participant_Survey:Race/ethnicity
phenotype:
  American Indian / Alaska Native, Native Hawaiian or Other Pacific Islander, Black or African American, White


human_id: hu5DD02A
date: 2012-07-19 11:02:30
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Hashimoto's Hypothyroid; CFS; neuropathic pain, allodynia, hyperalgesia; Inflammatory Bowl Disease; Remitting/reletting autoimmune inflammatory reactions; arthritis; temperature intolerance; pathogen-induced autoimmune disease.


human_id: hu22D7F9
date: 2012-07-31 00:33:17
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have been diagnosed with cancer 4 times with three primary cancers. In 1996 I was diagnosed with stage IIIB ductal carcinoma in my left breast. I was treated at Stanford with ACF followed by radiation and 6 months of CMF. The tumor disappeared without surgery.  Seven years later it recurred and I had an immediate mastectomy followed by Taxotere, Hereceptin and Cysplatin. In 2002 I was diagnosed with Stage 1 Lung Cancer and the midlobe of my right lung was removed.  In 2009 I had a malignant colon polyp removed.


human_id: hu22D7F9
date: 2012-07-31 00:33:17
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  I'm willing to upload medical records. If you can access Stanford and Palo Alto Foundation systems I can release files directly to you.  Otherwise I'll request a direct data transfer if possible. If that doesn't work I'll see what is possible.


human_id: hu8ABBF8
date: 2012-08-02 23:40:51
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  brain MRIs\nI have at least one, which was done recently, and have had two more done as part of a study that I might be able to get.


human_id: hu97762A
date: 2012-08-03 17:48:45
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Myalgic Encephalomyelitis (ICD-9-CM code 323.9)\nDysautonomia (Postural Orthostatic Tachycardia Syndrome & Neurally   Mediated Hypotension)\nPrimary Immune Deficiency (undetectable IgA)\nchronic Lyme disease (neuroborreliosis)


human_id: hu97762A
date: 2012-08-03 17:48:45
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  abnormal SPECT scan\nmodified tilt table testing\nmultiple IgA <6\npositive serology & PCRs for tick-borne and other infections\nLMW protein in RNase-L


human_id: hu616CCD
date: 2012-08-05 12:40:47
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Morbid Obesity I toped at 500+ pounds. Had a Gastric Bypass in 2000. Saved my life, but today, I am back up to 420.\n\nThis runs in my family along with Adult Diabetes. Grandmother, mother, her brothers and sisters (only 3 of 7 still living)


human_id: hu140B91
date: 2012-08-07 17:55:31
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Rheumatoid arthritis/auto-immune disorder triggered by gluten sensitivity (I am DQ2).  I have been diagnosed with RA.  My maternal aunt had RA.


human_id: hu174334
date: 2012-08-10 16:33:48
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Hospitalized for Stevens Johnson Syndrome 11/09, followed by DVT and hospitalization 12/09.\nSubsequently developed squamous cell cancer , with two surgeries right groin cancer.  A pathologist did sample of  cancerous specimen and Genzyme report showedEMA                           Epithelial Membrane Antigen (E-29)\nGCDFP-15                 Gross Cystic Disease Fluid Protein 15, Breast, Salivary Gland\nS100                            S100 Protein, Nerve Sheath Tumor, Melanoma, Chondrocyte \nTTF-1                         Thyroid Transcription-1 Lung and thyroid Carcinoma \nP63 (Pab 1801)           Mutated Tumor Suppressor Gene (PAb1801)  \nSubsequent Cisplatin and full pelvic radiation-developed Cisplatin toxicity and radiation internal and external burns. Questions remain-inherited bullous disease or ?


human_id: huAB8ED9
date: 2012-08-10 17:31:48
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have Bipolar Disorder which I believe is genetically rooted in the fact that mother and father are both alcoholics as well as my mother's father.  Suicide is very high in my family.\n\nI also have Hashimoto's autoimmune which I believe is also related to my family's weight issues, GI disorders, ADHD, alzheimers, HELLP syndrome, and sensory processing issues.


human_id: huD7960A
date: 2012-08-24 18:48:34
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have been diagnosed with hypokalemic periodic paralysis, which affects about 1 in 100,000 people. HypoK-PP is an ion channel disorder that dangerously manifests with the use of hospital medications but also in response to food and the body's own internal chemistry. \n\nAbout 70% of HypoK-PP patients have a known genetic mutation. I am in the 30%, where the mutations are not found yet. My variant was said to be "new" in that it frequently includes a loss-of-consciousness component as well as paralysis and weakness in the episodes. \n\nIn HypoK-PP, an abnormal amount of potassium shifts into the cells, losing the potential difference that the cells need to function. It means that muscles can't contract in a full blown attack or can't easily contract in a partial attack. In my case it includes daily paralytic and weakness reactions to food, and dangerous unexpected paralytic responses to medications in the hospital, for instance, where I am unexpectedly paralyzed and unable to move, including breathing muscles. \n\nI could not call out, gesture or push a button to tell anyone that I was in trouble. Luckily, unknown to me, my oxygen status was being monitored. After I lost consciousness due to anoxia, the team came in and provided mechanical breathing assistance. My breathing was not back to normal for several days. This is not the only hospital emergency like this that I have experienced -- this team was trying their hardest to avoid this type of problem, but we had the problem anyway. \n\nEpisodes started in my late teens (1970) in response to food, where I would become incapacitated for 72 hours (three days) after many of my meals. With a carefully controlled diet, I was able to shorten the episodes, but not eliminate them. \n\nOn a Holter monitor (in 2009) the EKG components of my episodes were measured. Starting in a fasting state, my EKG is normal, or even good, with a pulse rate of about 59 beats per minute. Within a half hour the episode is apparent, with many PVC's (premature ventricular contractions), other arrhythmias, and then tachycardia, going up to a resting pulse rate of about 128 bpm. The EKG's also showed breathing difficulty. \n\nThat day the episodes resolved in about five hours, where the pulse rate slowly came back to normal. But then a new episode came on because it was time for the next meal. So the 24 hour Holter showed 15 hours of abnormal EKG's, in response to food, slowly resolving in five hours each, that day. \n\nI am otherwise very healthy, but these daily episodes are very bothersome and severely limit my quality of life.


human_id: huD7960A
date: 2012-08-24 18:48:34
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  1. I have excerpts from the 2009 Holter data that show the EKG's in response to food. \n\n2. I have strength tests over time, first without HypoK-PP medication and then with HypoK-PP medication (walking speed on elevated treadmill, etc.) Many of these medications become ineffective after about about six to twelve weeks. \n\n3. Finally, I have extensive results from a "provocative test" that was performed in my cardiologist's office. \n\nIt is similar to a modified glucose tolerance test, where carbohydrates were ingested, and then, over time, various measurements are taken. \n\nMeasurements included strength (walking speed on treadmill), serum glucose, serum insulin, serum potassium, also comments by cardiologist over time. \n\nThere were some very unusual results -- my fasting insulin levels started at about 8% of normal (I started at around 0.6 microunits per ml, where normal fasting insulin is about 7.0 microunits per ml). After ingestion of glucose, when the insulin levels first rose to be about 1 microunit per ml, I lost 1/4 of my walking speed, and was barely able to walk by the time insulin levels rose to 5 microunits per ml. In normal subjects, postprandial insulin levels can easily go up to 140 microunits per ml. Mine rose up to about 35 microunits per ml. \n\nI was not "ok" again until the insulin levels fell down below 3.0 microunits per ml. \n\nThe potassium shift into the tissues, out of the blood, was documented in response to the glucose ingestion, falling from 4.2 mEq down to 3.5, and then coming up to 3.9 -- all in the normal range. There were PVC's and arrhythmias during the test, too. \n\nThis was not a severe attack, since I could still walk and did not lose consciousness -- in other attacks I can't move at all and also lose consciousness. \n\n


human_id: huF40410
date: 2012-08-26 13:42:24
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Glycogen Storage Disease Type V (McArdle's Disease), autosomal recessive related to the PYGM gene responsible for creation of phosphorylase enzymes in skeletal muscle cells.  Prevelence in the general populations estimated as 1 in 100,000, though rate of diagnosis is only 10-15% of that figure.  First symptoms encountered around age 5-7 (severe leg cramps), diagnosis not made until age 28 (but not for lack of trying, darn it).


human_id: hu75BE2C
date: 2012-09-03 14:40:13
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  2012/Sep/03\n\nI submitted the following information via the web page at https://spreadsheets.google.com/spreadsheet/formResponse?hl=en_US&formkey=dHRaNUxmUHdVaktxZXdsRlVyMlIwUUE6MQ&ifq\n\nI must have an unusual genetic characteristic. No one with whom I have ever discussed the issue experienced the earth's magnetic field, etc. in the same way that I have. People who experience it differently probably imagine that I am insane.\n\nEveryone must be sensitive to electromagnetic forces to some degree, e.g., when an electrical current or bolt of lighting runs through their bodies. If our cells were not sensitive to electro-magnetic forces, could our muscles contract, or our brains think?\n\nI must be extra sensitive to electromagnetic fields and forces, possibly in the same or a similar way that whales, homing pigeons and other animals that must migrate great distances across the earth are.\n\nI have travelled in over seventy countries, e.g., deep into equatorial forests, I have never felt lost. I always know where I am and how to get home.\n\nWhen I was a child swinging back and forth in a swing caused me to feel as though my entire body was being tickled. The sensation was unbearable. I thought every child felt the same sensations. Later experiences caused me to ask other people if swinging back and forth caused their bodies to tingle when they were children. All of them have replied NO.\n\nMany years later I sensed the heavy electro-magnetic forces that were building up in the atmosphere around me a few seconds before a mild bolt of lighting ran through my body. That lighting exited via my feet and some metal tools that I held in my hands (my fingers remained sore for a long time afterwards).\n\nI wonder why I inherited these unusual characteristics. I am interested in genetic genealogy. My DNA tests and those of my cousins show that nearly all of my ancestors were Celts and Vikings from Scotland and Ireland. The Vikings sailed to America centuries before Columbus. I wonder if evolution caused them to develop some of the same genetic characteristics that whales, etc. have.\n\nI bought a cheap cell phone a few years ago. I do not know if it was defective. My hands tingled when it rang or transmitted signals to the tower. The first and only call that I ever made via that cell phone lasted 52 minutes. Towards the end of that call I felt something creeping up the left side of my head (where I held the phone). The sensation became so awful that I ended the call without saying Goodbye. The left side of my head hurt so bad that I thought that I had a toothache or flu infection at first. The pain became unbearable and lasted for many years. My left eye stopped blinking. I am no longer able to focus my left eye. A large scab developed where I held the phone. The skin where I held the phone was discolored. I had tinnitus for years. The tissues in the left side of my head were damaged in other ways too. I shall not bore you with all the details.\n\nI hope that whatever genes caused me to be so sensitive to electromagnetic forces will be discovered so that people who inherited them can be made aware of how cell phone use may affect them.\n


human_id: hu718EB2
date: 2012-09-13 20:57:29
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Diagnosis of Discoid lupus erythematosus; have not yet been tested for SLE. Immediate family history includes autoimmune diseases such as non-hodgkin's lymphoma and thyroid disorders.


human_id: hu718EB2
date: 2012-09-13 20:57:29
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  Two Skin Biopsies - Dx ICD9: 695.4 (Discoid Lupus Erythematosus) & 238.2 (Neoplasm uncertain behavior Skin). Also have preliminary results from Pathway Genomics Health Condition Report indicating three associated SLE related genes/variants: (ITGAM, rs1143679, G/G), (PTPN22, rs2476601, G/G), and (STAT4, rs7574865, T/G).


human_id: huF5D986
date: 2012-09-19 14:14:07
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I think I might have a rare genetic condition that has to do with how my immune system functions because I have been plagued with several diseases and serious conditions throughout my life and I am very sensitive to foods, drugs, lotions, perfumes, my own sweat and many external and internal substances, listed below:\n\nage 14-17: 2 very large juvenile fibroadinoma tumors in my right breast\nage 26-32: Onset of severe food allergies to dairy, eggs, sugar, mushrooms, bananas, dx with Hashimotos Thyroiditis, Malignant Melanoma x2, Swine Flu and several other severe colds, flues and itises (Bronchitis, tonsillitis, etc). If someone with a cold comes near me or I touch something they touched, i will get sick.  Autoimmune diseases run in my family as does cancer of many kinds.


human_id: huF5D986
date: 2012-09-19 14:14:07
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  Cancer: I have surgery pictures and lab tests for both my Melanoma surgeries.\n\nBreast Tumors: I have the surgeons notes and draw up of my tumors.\n\nHashimotos Thyroiditis: I have lab tests that prove I have the titers.\n\nColds, Flu & allergy: I have several chest x-ray results, colonoscopy results and images, allergy blood and skin testing results, ultrasound results, and several other blood tests done throughout my 20s and 30s.


human_id: hu16FFF2
date: 2012-09-25 20:21:47
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  HHT or formerly called Oslo-Weber Disorder.  Its main symptoms include nosebleeds as well as tiny pink spots (blood vessels) on the skin.  As you age, the condition worsens.  It can aversley affect the brain, heart, lungs and liver.\nPomagranate seems to aid in reducing the nosebleeds.  I am currently taking 500mg of pom extract daily.\n


human_id: hu5FA322
date: 2012-09-26 16:28:03
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Poor detoxification -  have NULL  GST-T, GST-M, mutant CYP450-2D6 (ext metabolizer), CYP450-2C19 (poor metabolizer), \nCYP450-2C9 (ext metabolizer), NAT2 catalytically inefficient\n\nHave symptoms of "portal systemic encephalopathy" including 4-6 Hz EEG "spike & wave"\n\nfamilial Aortic Aneurysms


human_id: hu5FA322
date: 2012-09-26 16:28:03
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  The genetic data on CYP450s, Nat2, GSTs - can't figure how to upload the\npicture of the EEG "spike and waves"  - we're trying hard to get my exome done.


human_id: hu8622BD
date: 2012-09-30 15:22:41
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  kidney cancer, my maternal uncle also had kidney cancer\nthyroid nodules, my mother, maternal aunt, maternal cousin have this


human_id: hu519DE2
date: 2012-10-01 17:44:41
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  results of histology after right knee arthroscopic surgery 4/23/12 confirmed diagnosis of synovial chondromatosis, am awaiting same result from arthroscopic surgery on left knee on 9/21/12


human_id: hu0E4BBC
date: 2012-10-01 20:10:11
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Can't drink or smell alcohol without severe physical effects.  Severe effects from cigarette smoke.  Become very addled mentally when pregnant.


human_id: hu04693B
date: 2012-10-04 22:09:07
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Charcot Marie Tooth (not sure if this counts as severe or not) *answering about CMT\nWas diagnosed with Polycystic Ovary Syndrome by one general practitioner, but a second GP was not convinced.


human_id: hu774230
date: 2012-10-09 23:01:24
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I am undergoing testing to determine whether I have celiac's disease or a gluten sensitivity. Based on family health history, my doctor suspects celiac's. I am currently waiting on the results of my gluten challenge and following egd/biopsy.


human_id: huED0F40
date: 2012-10-12 06:29:29
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  My 11-year-old son was just diagnosed with scoliosis, becoming the third generation diagnosed with spinal malformation. My son also has periodic low HDL in blood draws. While researching causes of kyphosis to prep for my son's fall 2012 orthopedic evaluation, I discovered Marfans Syndrome, Ehlers-Danlos and other genetic connective disorders for the first time. Since early childhood, I could bend my thumbs and hand far back, pop both my knee caps in & out of joint, and I could wrap my legs into a lotus position and then lift my crossed legs to touch my chest, multiple times like a seated situp. My father's 1995 severe mitral valve prolapse echocardiogram with enlarged aortic stem, his (and my) history of early arthritis detected in the spine, his very low body weight (143 - 150 lbs almost all of his adult life (until it went lower in his 60s) despite being 6'4" with long slender limbs & fingers, and a family history among uncles of hip dysplasia, multiple hiatal and inguinal hernias and chronic pain all made sense related to a connective tissue disorder: either Marfans or EDS. My geneticist visit is not until Spring 2013 at Johns Hopkins Hospital, but my Aug/Sep 2012 opthamologist, cardiology, radiology tests are all showing signs of connective tissue disorder of some kind, more like Ehlers-Danlos in my case (I.e. no aortic stem enlargement on my own 2012 echogram and only mitral valve degeneration, not full prolapse-- my father was 66 when his first echo was done and he died before a followup was done.). Most of the men on my father's side of the family tend to die months ahead of or after turning 67, despite different levels of healthful behavior, levels of medical care, etc. going back to the 1920s, as though parts have "worn out" at that age.


human_id: hu9D3638
date: 2012-10-12 12:25:23
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Well, maybe it's not that rare, and definitely not severe, but potentially important for the health of many people.\n\nI have IgA deficiency.


human_id: hu9D3638
date: 2012-10-12 12:25:23
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  I think I can my providers at Harvard University Health Services to send me an electronic copy of my blood test results. From the negligible (undiscerably low) IgA count reading, the diagnosis is obvious.


human_id: hu174334
date: 2012-10-12 16:43:40
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have had many severe adverse reactions to Rx and supplements including, Stevens Johnson Syndrome, DVT, 12 squamous cell skin cancers, 1 basal cell skin cancer, 2 right groin squamous cell cancers.\nAlso genetic CAD but with PAD.


human_id: huBAA265
date: 2012-10-12 20:51:47
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I was born with the rare congenital non-spherical hemolytical anemia, that was corrected several years later via multiple blood transfusions.\n\nRelated to that, we believe I have one or more types of Porphyria.  It has not formally been diagnosed due to the difficulty in maintaining viable biological samples.  I have had my blood studied by the lab at Mt. Sinai Hospital, but they did not find that I had a mutation previously documented,  They did not do a sequencing of my genes.\n\nI am a carrier for Hemochromatosis, which is strongly linked to one of the skin varieties of porphyria, PCT.  I have symptoms consistent with PCT, as well as EPP (another skin type, associated with congenital hemolytic anemia), and HCP, one of the acute porphyrias.\n\nI have Wolfe Parkinson White Syndrome, a hereditary electrical disturbance in the heart, which has been corrected via ablation surgery.\n\nI have other health problems, but these are the ones that are more severe and rare.\n\n


human_id: huBAA265
date: 2012-10-12 20:51:47
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  I have the records from my birth, that discuss the hemolytic anemia.  The records had to be obtained from the naval hospital archives and are limited to a few pages of test results.\n\nOn the porphyria, I have very little, other than confirmation by the recognized expert on the subject,  Dr. Anderson from UTMB in Galveston, who said that my symptoms leave a strong suspicion of porphyria.  I have the negative genetic results from Mt. Sinai, which are not conclusive, since there are many unique mutations of Porphyria that have not been documented, due to limited availability (only Mt. Sinai in the US), the high cost of testing, and the fact that many may not even know about Porphyria to seek diagnosis.\n\nOn the WPW, I'm sure I could obtain an electrocardiogram that shows the unique electrical wave pattern of the disease.  Or something more from my cardiologist.  It was successfully ablated, so I no longer have it.  My maternal aunt also had WPW that was ablated.\n\nThe carrier status of hemochromatosis is noted on my 23andme profile.


human_id: hu0B100A
date: 2012-10-16 22:57:56
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Capable of voluntary shoulder subluxation. (this will be answered for)\nHomosexual male.\nADHD.\nLeft-handed.\nBlue-eyed.\nCannot taste phenylthiocarbamide.\n


human_id: huB5A0DF
date: 2012-10-17 23:35:01
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Heteroplasmy - I am not sure if this falls under a rare trait but feels it needs to be mentioned here for research purposes.  I have read that it was once considered very rare but as more genomes are sequenced it is becoming more common.


human_id: hu569A8F
date: 2012-10-18 09:20:26
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Multiple Sclerosis.  I, like everyone else, do not know if there is a genetic cause or a possible genetic and environmental combination. Not sure if MS is considered a severe disease in all cases, either


human_id: hu42F87B
date: 2012-10-20 23:41:51
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I was diagnosed with MS in 1988.  Recently my neurologist has discussed the possibility with me that I may have a mitochondrial myopathy of some kind instead of MS.


human_id: hu592A16
date: 2012-10-24 21:11:14
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Hughes Syndrome (antiphospholipid syndrome) My mom had multiple sclerosis. I strongly believe the two are genetically linked.


human_id: huB9F2F3
date: 2012-11-14 09:30:39
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  There are autopsie results from biopsies for myself, my mother and my sister.  My maternal uncle also had melanoma -


human_id: huE57FEC
date: 2012-11-19 17:50:24
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  The diagnosis was made in 1992, and confirmed at a medical school teaching hospital in 1994. Although the records are old, my understanding is that the data is still available, but it might take a while to get it.


human_id: hu76CAA5
date: 2012-11-22 15:41:16
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Atrial fibrillation with rapid ventricular response. Currently dependent on propafenone to suppress the malignant. Recurrence of atrial fibrillation invariably leads to rapid ventricular response requiring emergency cardioversion (will not convert with IV medication regimen). The invariable rapid ventricular response is the component that distinguishes it from "typical" atrial fibrillation. Atrial fibrillation is always malignant for me, which is why I am dependent on propafenone extended release (a very expensive medication) versus anticoagulation with Coumadin. The Coumadin can reduce the  stroke risk, but does nothing to control the tachycardia of 130-140 associated with the atrial fibrillation. I live a normal life as long as I have access to the propfenone extended release. This may be a problem in the near future.


human_id: hu76CAA5
date: 2012-11-22 15:41:16
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  Two full reports by cardiologists of emergency cardioversions. Another report available by submission of a HIPAA request form.


human_id: hu8A5FBF
date: 2012-11-28 20:50:45
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Ulcerative Colitis (extremely severe pancolitis)(replies below apply to this condition)\n\nOther Current:\nDry Macular Degeneration \nProstatic Hyperplasia\n\nOther Past:\nAsthma\nMelanoma\n


human_id: hu8A5FBF
date: 2012-11-28 20:50:45
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  Medical records from Stanford Hospital\nMedical records from Palo Alto Medical Foundation\nSeries of colonoscopies (images and reports)\n\n(*) I can give both Stanford and PAMF permission to release my records, and I also have some of the reports/images in CDs.


human_id: huCD90E3
date: 2012-12-03 05:15:05
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  All of my paternal male relatives have a significant amount of body hair compared with other caucasians.


human_id: huF8D320
date: 2012-12-06 14:50:40
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have ulcerative colitis. I think that it is genetic, because there are people with inflammatory bowel diseases on both sides of my family.


human_id: huD09050
date: 2012-12-13 15:36:54
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  1. Pyloric stenosis (answers below pertain to this trait)\n2. Polydactyly (no trait, but son and father have trait - I'm a carrier)


human_id: huB10361
date: 2013-01-09 13:24:32
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Ehlers Danlos with Marfans overlaps - CSF leak history (cranial) multiple small nerve root diverticuli throughout spine- low IgM (25)- I wasn't diagnosed until 2010 (previously was dx'ed with lupus with Behcet's features).


human_id: huB10361
date: 2013-01-09 13:24:32
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  several geneticists' clinical reports- overlaps with symptoms/hypermobility- my disease progression is more severe in downward spiral than most- we do not know WHICH type of EDS I have and/or if I have a concomitant neuromuscular or autoimmune etiology.


human_id: hu101EF8
date: 2013-01-25 23:22:10
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I had Rheumatic Fever as an adult.  I was about 33 years old.  Was hospitalized for 6 + weeks.  No permanent heart damage.\n\nI was diagnosed with Myasthenia Gravis in Feb 2004 at age 71.  It was quickly controlled by drugs.  However, in April 2004 I was bitten by a dog, which was never captured.  Thus, I had to have the rabies shots.  This activated my MG & I ended up in ER with breathing difficulties.  I am now (25 Jan 2013) w/o symptoms & off all medications for MG..


human_id: hu17EA24
date: 2013-01-30 22:40:03
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  specific inability to navigate- developmental topographical disorientation. I cant find my way around in even the most familiar places. I get lost going to routine places and cant find my way around inside buildings. This has gone on since I can remember, and another sibling is similar. \n\nI have also been diagnosed with bipolar disorder, but that is the more 'normal' abnormal trait.


human_id: hu8B2C08
date: 2013-02-03 13:56:10
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Hashimoto's Thyroiditis, autoimmune disease although not sure how "severe" it is, medication is required for the lifetime of the individual after diagnosis. I have a half brother on my mother's side who also has this diagnosis; my mother is hypothyroid but not necessarily Hashimoto.


human_id: hu8B2C08
date: 2013-02-03 13:56:10
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  03/1/12 21:48\n\tMilne-Krohn\treviewed. thryoid peroxidase was positive. this is the antibody that is high with hashimoto's thyroiditis (the autoimmue disoder that commonly affects thyroid labs). youw ill likely need thyroid meds long term.    \n\n\n\nLABCORP \n\nCOLLECTED: 02/29/12 00:00 \nRECEIVED: 02/29/12 23:11 \nREPORTED: 03/01/12 08:21\t\tREPORT STATUS: FINAL \n\nTest Name\t In Range\tOut of Range\tReference Range\nLab\n\nThyroid Peroxidase (TPO) Ab: Final\n\tThyroid Peroxidase (TPO) Ab\t\t142 H\t0-34 IU/mL\t01\t\n\n\n01: LabCorp Herndon, 13900 Park Center Road, VA, Herndon 201710000


human_id: hu22577A
date: 2013-02-04 15:28:00
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Type 1 diabeties\nConcomitant:\n  HLA markers \n  Glaucoma and macular degeneration \n  Neural issues (Dad had ALS- and Essential tremors)  essential tremors\n  Advanced Kidney disease\n  3 stent/heart


human_id: huEAE6C8
date: 2013-02-12 21:44:30
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I'm not sure how you define "severe", but I have been diagnosed with PCOS, bipolar disorder, fibromyalgia, and am in the process of being diagnosed with Aspergers Syndrome (HFA).\n\nt is my feeling that everything stems from a neurological/hormonal problem (HPA axis) like hypothalamus problems, but I have no real evidence of this.  Oh, and I identify as "asexual" which means I am not sexually attracted to anybody (for the most part) and in my case that I have virtually no libido.\n\nFor the purpose of this survey, I guess I'll use fibromyalgia.


human_id: huEAE6C8
date: 2013-02-12 21:44:30
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  I use patient gateway so I have copies of some of my lab results.  I am willing to provide any information that I can easily obtain.


human_id: hu580F49
date: 2013-02-18 12:54:26
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Food intolerance to artificial food coloring/preservatives. Causes severe stomach discomfort, and may include sweating, fainting, paleness, and headaches depending on the amount consumed.


human_id: huB89823
date: 2013-02-18 18:07:56
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  depression (chronic clinical, formally diagnosed and difficult to treat)\n\nasthma (with apparent airway remodeling, difficult to treat in childhood, and relatively stabilized in adulthood)\n\n


human_id: huB89823
date: 2013-02-18 18:07:56
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  For Depression: clinical notes / medical records\n\nFor Asthma:  spirometry test report and medical records


human_id: hu3AAA9E
date: 2013-02-26 17:52:33
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  HSV1 - father, aunt, cousins have this. Mine appears on my left eyebrow. First outbreak was in 1995, I was 8 years old.


human_id: huD94CBF
date: 2013-03-03 22:13:07
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have bipolar disorder. I have been hospitalized multiple times for it. I am considered 70% disabled by the VA, and also disabled by the Social Security Administration.


human_id: huAC3640
date: 2013-03-06 01:13:03
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Trait - Beginning approximately at puberty.  I believe it to be possibly metabolic in nature.  I am unsure as to the possible severity, and even whether it is all related, but I am suspicious as my teen daughters seem to be following in my footsteps.  Doctors seem relatively unconcerned.\n\nBeginning at puberty, I would feel extremely ill in the early mornings especially if I did not get enough rest - my youngest daughter vomits repeatedly and violently under the same conditions.  If genetic, she has it worse than I.\n\nAlso beginning at puberty, I have been unable to eat sugars on an empty stomach.  To do so results in a severe drop in blood sugar a couple of hours later, even to the point of near loss of consciousness when younger.  I never knew anyone who reacted as I do until my oldest daughter reached puberty and the same happened to her.  It continues occasionally to happen to her and I worry constantly as she has had some really bad spells that she had a difficult time pulling out of.  \n\nFinally, throughout my lifetime I have had numerous unexpected reactions to various drugs, and I have had several unexplained losses of consciousness in the past few years, one especially severe that resulted in a head injury/fall.  These do not, however, seem to be linked to blood sugar issues as it was measured at 110 at the hospital immediately afterwards.\n


human_id: hu02BA92
date: 2013-03-06 07:12:40
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have a number of different serious disease processes that I believe may be a single genetic predisposed entity. Liver disease in the form of hepatitis c and with cirrhosis, NASH, but I had NASH before the hep c. I also have splenomegaly, portal hypertension, peripheral artery disease, peripheral neuropathy, enlarged heart, diabetes 2, ADDHD


human_id: hu097A26
date: 2013-03-13 14:42:55
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Highly likely genetic predisposition to patelae abnormalities, me, my mother, and my mothers sister have patelae that dislocate, though the severity differs by person. I have the worst symptoms. There has been no formal diagnoses, just treatment via surgery and lifestyle adjustment.


human_id: huC93609
date: 2013-03-13 14:52:46
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  I have already done some genetic testing as well as have significant amounts of radiological as well as pathological documents demonstrating the disease as well as the growth patterns which appear to be different the most people with the "typical" carcinoid/neuroendocrine disease profile


human_id: hu09D626
date: 2013-03-14 12:33:27
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  1) clinically diagnosed as having Ehlers-Danlos Syndrome\n2)  was told I had a Emery-Dreifuss Muscular Dystrophy recessive(?) gene - something about SNP 'rs61046466' in the gene 'LMNA  lamin A/C'\n\nno biological family medical history after birth, but I have had strange symptoms since I was a baby but mainly once I started walking.\n


human_id: hu09D626
date: 2013-03-14 12:33:27
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  I don't have any genetic testing or documentation for EDS, all documentation in clinical and experience related.  this was diagnosed by a doctor and in my medical history.\n\nas for the EDMD, this was just brought to my attention when my raw genome data from 23andme was run through openSNP.  i was told that i had many rare/uncommon SNPs including one linked to EDMD.  I have uploaded this raw data.


human_id: hu756D3A
date: 2013-03-21 15:40:22
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Autoimmune liver diseases: *Primary Biliary Cholangitis (or sometimes Cirrhosis), Autoimmune Hepatitis, Porokeratosis


human_id: hu618103
date: 2013-04-02 13:00:49
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  PDF record transcript from Mass General including muscle biopsy results, lab work, and clinician's notes.


human_id: huEBA8B1
date: 2013-04-09 13:14:52
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Auto immune variously diagnosed as lupus, Crohn's, Sjongren's, Psoriatic Arthritis, Spondyloarthropathy, inherited from mother's side\n\nOrthopedic and soft tissue anomalies including cervical ribs (from father's side), possibly involving the warping of my right hip structure,  and an oddly placed appendix - traits shared by other family members


human_id: huEBA8B1
date: 2013-04-09 13:14:52
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  I'll have to dig into my medical records, mostly office notes and some surgical notes, to see if any of them contain mention of the orthopedic anomalies.


human_id: hu51322A
date: 2013-04-11 13:45:50
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have rheumatoid arthritis and would love to participate in any study that would identify the genetic markers for this disease.


human_id: hu19B7A0
date: 2013-04-17 02:30:21
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  CT scans of onset of disease, blood lab results for 8 years, PANCA and ASCA gene testing, colonoscopy and endoscopy images


human_id: huAF9B09
date: 2013-04-17 03:24:08
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  several colonoscopies, endoscopy, and each year I get my blood tested for a comprehensive metabolic panel, CRP, sedimentation rate, CBC


human_id: huE11A1A
date: 2013-05-16 17:46:08
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  My clinical diagnosis of Young Onset Parkinson's Disease was made in November of 2011.  I have Clinic Summarries from my neurologist (a movement disorder specialist) as proof, but otherwise they are not particularly interesting.


human_id: hu911FDC
date: 2013-05-18 18:51:17
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have had acute attacks with severe abdominal pain, nausea, vomiting, severe peripheral neuropathy, muscle weakness, seizures, hallucinations, rapid heart rate, severe constipation and/or diarrhea, insomnia, paralysis of gut (food does not move through system). The acute attacks can be caused by stress, infections, alcohol consumption,certain drugs, fasting or even something as simple as being in an elevator with a person wearing strong perfume or other things like car exhaust or bus fumes. My urine becomes fluorescent orange and if placed in sunlight my urine darkens to the color of coke.


human_id: hu3F13EF
date: 2013-06-03 00:02:35
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I was diagnosed with myopia at age 7, probably had onset at earlier age.  Myopia has been progressive throughout life.  Astigmatism started in 20's, both eyes. Left eye is -6, right eye -6.25.\n\nPresbyopia started as inability to see "near" with contact lens correction of myopia, but very-near acuity remains excellent without contact lens or glasses.


human_id: hu3F13EF
date: 2013-06-03 00:02:35
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  Not directly relevant to myopia, but I do have optic nerve imaging and eye pressure measurements to contribute.  I will need to get the documentation from my ophthalmologist.


human_id: hu1CCE96
date: 2013-06-03 21:40:34
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Autonomic Nervous System Dysfunction (Postural Orthostatic Tachycardia Syndrome), Connective Tissue Disorder & Raynaud's


human_id: huBD8A03
date: 2013-06-20 17:48:29
phenotype_category: Participant_Survey:Disease/trait: Documentation description
phenotype:
  My MRI's show no lesions. I have had a spinal tap test positive for oligoclonal bands. Neurologists at several hospitals say it is a rare benign form of MS. I have had limb numbness from my toes to my waist. I have also had optic neuritis. I can produce these records if needed.


human_id: hu52B90E
date: 2013-07-20 19:33:05
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  *Epileptic seizures between age 0-2years.\n*Phenobarbital age 2-5years\n*No seizure occurrences since.\n*Age 30yrs awaken immobilize.  All test were normal. Muscle relaxers and narcotics returned me to my previous normal.  Realization: living with pain and lethargy is abnormal.\n*Age 33yrs take Bactrim for 10 days and feel wonderful.\n*Begin "Anti-folate" diet.  Take metholated-folate multi-vitamin.  Pain reduction and lethargy improvement.  \n*Genetic test MTHFR is normal.\n*Positive experience with Beano: alpha galactosidase.  Begin taking 50 beano per day with positive results.\n*Anderson-Fabry disease test is normal.\n*Well being continues to be unstable.\n*Realize carbohydrates are the culprit; folate is innocent.\n*Purchase and test:Fructose, Dextrose, Lactose. Fructose is sharply and swiftly painful.  Dextrose is less severe.  Lactose seems benign unless taken in high doses.  *Determine any complex carbohydrate or vegetable/fruit is painful and tiring.\n*Try conversion to meat/fat diet.  After 10 days I felt compelled to take lactose.\n*Preliminary tests are negative for Glycogen Storage Disorder Type 7 phosphofructokinase.\n*New hypothesis: Genetic Disorder of Glycosylation.\n


human_id: hu8DDB68
date: 2013-07-28 22:37:52
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have or had before I donated a kidney, a bilateral duplicated collecting system. (Not sure if that is rare or not)


human_id: huF5E454
date: 2013-07-31 15:02:51
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I am a carrier for several diseases.  I don't know if you need that info but if so, I am a carrier for Cystic Fibrosis and Tay-Sacs. I have already completed an initial DNA testing with 23andme.  I am happy to share all of that info with you guys.


human_id: hu4D1CC2
date: 2013-08-07 00:32:58
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  My mother was adopted and doesn't know her biological parents or heritage, so my maternal side is quite vague. My father is not, nor has ever been, in my life so I know very little of his heritage. My mother is diagnosed as bipolar and there is some history of eczema that runs on my father's side. Other than that I have no knowledge of my family history.\nI do know, however, that I have a rare blood type, which is AB negative.


human_id: hu43294F
date: 2013-10-01 06:20:29
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Supernumerary Kidney- Two kidneys with two ureters opening separately into bladder.\n'AG'\t- rs72653744\tABCC6  ATP-binding cassette, sub-family C (CFTR/MRP)\nmtDNA Haplogroup H1bm\n'TT'\t- rs34548758\tCASR  calcium-sensing receptor\t\nI have Lupus, Chiari 1, Sjogrens, Raynauds, Spinal Stenosis as well as other congenital anomalies, Spina Bifida Occulta...off the top of my head.\nMy family has Lupus, Polyglandular Autoimmune Syndrome, Hashimoto's, Graves, A fib, Autoimmune Hepatitis, Hyperparathyroidism, Type 1 & 2 Diabetes, Meniere's, Congenital Heart Defects...others.\ngs192, gs250, rs4680(G;G), rs1800566(T;T) - + many other cancer risks


human_id: huAD225A
date: 2013-10-17 02:14:24
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Genetic Traits:\nAttention Deficit Hyperactivity Disorder (ADHD) is genetic from my paternal lineage as well as hypertension. \nI have been diagnosed with Early Onset Dysthymic Disorder.\n


human_id: hu3891E3
date: 2013-11-07 20:54:04
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Severe Family history of schizophrenia on both sides of family. in parents generation, four of seven diagnosed


human_id: hu61F3D9
date: 2013-11-08 12:13:33
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Mother has a rare form of glaucoma. Optic nerve degeneration w/o increased pressures. Don't know if I have it though.


human_id: hu155D20
date: 2013-11-10 20:56:05
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  No severe genetic diseases/rare genetic traits. According to my 23andMe data, the only genetic disease I have a significantly higher proclivity for (4.2x higher) is venous thromboembolism. I am heterozygous (CT) in the rs6025 SNP of the F5 gene/region and have A+ blood type.


human_id: hu9AB964
date: 2013-11-11 23:52:49
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Recently I was found to have somewhat elevated blood bilirubin levels, but otherwise normal liver enzymes, suggesting Gilbert's syndrome. This has not been directly confirmed genetically.


human_id: huECF94A
date: 2013-11-12 13:13:47
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  family history of profound early onset hearing loss.    me included\n\nHLA-B27     have psoriatic  arthritis and/or ankylosing spondylitis


human_id: hu35020C
date: 2013-11-15 22:33:07
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  4 generations of cancer on Father's side: colon, intestine, melanoma.  Radical hysterectomy for one sister, colon and ovarian for one cousin, melanoma for one male cousin


human_id: hu294056
date: 2013-11-16 02:34:22
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Ehlers Danlos type not yet know. I have had a blood draw to type it and also check for hereditary aortic dissection since my Father died at age 35 due to aortic dissection.


human_id: huB11146
date: 2013-11-19 14:32:02
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I Frequently (weekly) suffer "Stomach" Complications and Pain.(Un-Diagnosed) I had Ulcers (diagnosed) at an early age of 13 years old (3-4 Ulcers) diagnosed and had an endoscopy at the time. My paternal family also had history of Stomach Complications and Stomach pain and a history of Alcoholism and Depression. My maternal family has History of Heart complications and Alzheimer's.


human_id: huB11146
date: 2013-11-19 14:44:14
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I weekly suffer Stomach Complications and Pain (Un-Diagnosed). I had ulcers at 13 years of age (3-4 Ulcers)  and had an endoscopy at the time (diagnosed). My paternal family has a history of Stomach Complications and Stomach pain and a history of Alcoholism and Depression. My maternal family has History of Heart complications and Alzheimer's.


human_id: hu5325EC
date: 2013-12-07 02:15:13
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have a circadian rhythm sleep disorder, Delayed Sleep Phase Disorder.  I also suffer from idiopathic hypersomnia.


human_id: hu5C5920
date: 2013-12-07 10:48:28
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have Asperger's syndrome, I also have a genetic metabolic disorder (like or is a form of Porphyria.)


human_id: huC62047
date: 2013-12-23 21:06:37
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have had metaplastic carcinoma of the breast twice. Once in 2/12 and once in 2/13. This is a very rare breast cancer. I am BRCA1&2 negative and also have had the BROCA test with no known mutations detected. \n\nThe first tumor was:\n\nLow grad spindle cell metaplastic carcinoma arising from a sclerosed papilloma with and in situ squamous cell carcinoma component.\n\nThe second tumor was:\n\nMicroscopic examination reveals a malignant neoplasm, characterized by intermediate to high nuclear grade cellular proliferation. The tumor cells are predominantly spindle in shape and are focally arranged in short fascicles. In other areas they line irregular spaces leading to a pseudoangiosacromatous appearance. Immunohistochemical studies demonstrate strong immunoreactivity with cytokerartins CK AE1/3, CAM 5.2, CK 34BE12, CK 5/6 and p63 in the later areas and only focal staining in the spindle cell areas. The tumor cells are also strongly positive for vimentin, and negative for s-100, CD34 and SMA. \nProliferation index (Ki-67) is positive, 22% nuclear staining (Unfavorable).\nKi67 clone MIB (Dako).\nThe morphologic features and the IHC results are consistent with metaplastic carcinoma with areas of spindle cell carcinoma and squamous cell carcinoma, acantolythic viariant.\n\n\n


human_id: hu450107
date: 2014-02-05 11:44:38
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  My father's family is Ashkenazi and his grandparents immigrated to the US from Europe.  My mother was adopted and we do not know much about her biological ancestry.


human_id: hu28391C
date: 2014-02-25 03:02:21
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Not sure how rare it is, but I am affected by a deformity known as Hypospadias. Mine is not severe; I have normal to heightened orgasms and have produced two children (both sons). I only found out that it was not normal recently. I knew I looked different to other men, but did not know what was wrong. I went to a urologist for help with an enlarged prostate and trouble urinating and erectile dysfunction and he told me that my penis was deformed and explained what was wrong. I read about it on the Wikipedia web site and apparently it is not that rare, but there are severe cases that require surgery. I am uncircumcised or partly circumcised and I read that could have contributed to the problem. However, I think most are a birth defect.Perhaps you could shed some light on this or confirm or deny my findings.


human_id: huBAEEB0
date: 2014-02-25 14:03:48
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  History on maternal side, including my maternal grandfather, of massive heart failure and death pre- 60 years old.


human_id: huAE4A11
date: 2014-03-02 10:04:36
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  From when I was 8 years old until around age 18, I had a rare autoimmune neuromuscular disorder which was diagnosed as chronic inflammatory demyelinating polyneuropathy.  I have a paternal family history of other autoimmune diseases such as lupus, asthma, and eczema.


human_id: huCCF18D
date: 2014-03-02 11:29:47
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I carry a rare genetic mutation (D178N) on the prion protein gene (PRNP.)  This mutation (in cis with the 129M polymorphism) has been associated with familial prion disease.


human_id: hu9745B5
date: 2014-03-26 23:52:57
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  No. Parents both have congenital pre-disposals & conditions (mother: diabetes; father: heart defect, heart disease) but I do not have theirs. I was diagnosed Hypothyroid in 2008 following a month with limited sleep (I'm a corporate/civil attorney and had a large case-load with a lot of travel & had very little common sense about how lack of sleep could affect me), but am unaware of any family history on either side. I am height-weight proportionate, but not many others in the family are on both sides, so the pre-disposed conditions are checked, but have no surfaced.


human_id: hu816A0B
date: 2014-04-06 07:22:24
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Based upon my responses to an online screening quiz, I am most likely suffering from an obsessive-compulsive disorder.\n\n


human_id: hu5953A9
date: 2014-04-08 18:38:38
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I'm the only one in my family beside my paternal grandmother to have red hair between her 3 children and her 4 grandchildren of which all have come from my father/mother.


human_id: hu8A5FBF
date: 2014-05-02 17:19:51
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Genetic: HH carrier, CF carrier, some SNPS related to ILs.\nClinical (rare, but w/multifactorial causes): UC, SNHL


human_id: huEC3ADA
date: 2014-05-02 18:25:35
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I am theonkyhearing person n my family.  My parents, and both siblings are deaf.  My father lost his hearing at two, my mother, brother and sister have been deaf from birth.  My mother and sister have night blindness, low vision, and ataxia, but it is not Retinitis Pigmentosa, and is not Ushers Syndrome.


human_id: huFFA651
date: 2014-05-04 23:57:37
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Nothing diagnosed, but I suspect collagen or connective tissue irregularities and potentially autism associated genes.


human_id: hu02F2F9
date: 2014-05-17 20:04:31
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Yes, I have a mutation in PMS2, one of the genes associated with Lynch Syndrome.  My family history of colon cancer, and personal history of precancerous colon polyps, suggests that it is a deleterious mutation.


human_id: hu02F2F9
date: 2014-05-18 19:25:55
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I already completed this survey once, but forgot to mention that in addition to having a PMS2 mutation, along with a family history of colon cancer and a personal history of precancerous colon polyps, all of which points to Lynch Syndrome, I am also heterozygous for Fanconi's anemia.


human_id: hu566AA7
date: 2014-06-13 12:00:53
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Homozygous for risk allele for rs1061170(C;C).  Have chronic inflammation from environmental toxins (mycotoxins, etc) known as CIRS resulting in extremely elevated TGF-B1, C4a, and extremely low ADH, VEGF, MSH, and VIP as a result of a specific HLA DR/DQ combo.  Very well documented with thorough blood labs.


human_id: hu224941
date: 2014-06-17 10:04:44
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  It Mitochondria Myopathy (mtDNA) however it did not present until I was 40 after taking Lipitor which weakened my muscles.  This has been followed by 14 years of declining health, constant pain, and 10 or so operations for tearing of connective tissue due to the muscles inability to perform their tasks as designed.  I also have POTS, and there is a strong possibility that I other issues, and Neurologist at Mass General Hospital are debating a second muscle biopsy (first one in 2009 confirmed the mtDNA disease) they are also considering calcium channel blockers and seem flummoxed by the complexity of my presentation.


human_id: hu9D00EB
date: 2014-06-17 11:37:30
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  None that I know of.. Alarmingly healthy. Never even had any common childhood ailments except German Measles.


human_id: hu4E8403
date: 2014-07-07 12:52:04
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Possibly sending out this questionnaire before and after testing would give a good example of information also.  I was tested for numerous disorders for years prior to finding out what I had. I would like to see how close or correct testing prior to this would be.  Maybe one day this could be used in a better way, making  genetic testing a more streamline approach to finding answers to the more sickly faster or a preventative approach.


human_id: huB8B7C3
date: 2014-08-04 00:33:06
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  My father is heterozygous for E148Q mutation in the MEFV (FMF) gene, but it is unknown if I am a carrier of those specific genes.\n


human_id: hu5C14F0
date: 2014-08-23 09:57:10
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have partially webbed toes. When each of the four of us were born and released from the hospital, my father looked at our feet to know that he was bringing his own baby home.\n\nI learned from "23 and me" that I am in the top 1% of people carrying the most Neatherthal DNA. My husky grandfather is from Northern Italy.  If you saw me, (and how thin I am) you would laugh about it the way I do.


human_id: huC51695
date: 2014-08-27 14:23:04
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Have been diagnosed by geneticist with connective tissue disorder, probable Ehlers-Danlos. Still awaiting subtyping, which will be available in two weeks.


human_id: huACE510
date: 2014-09-08 23:00:54
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have Hartnups. This is a recessive metabolic disorder. Treatment  is high protein diet and niacin supplements.


human_id: hu16EC18
date: 2014-09-11 21:37:10
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have a tendency to bite my nails. My son is 3 years old and does it too. I'm pretty sure this was nature rather than nurture.\n\n


human_id: hu3AD9A6
date: 2014-09-13 21:57:01
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  An unknown form of muscular dystrophy, likely related to bethlem myopathy though negative for all markers.


human_id: huFF2969
date: 2014-09-14 16:12:48
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have three auto-immune conditions which do not appear in any members of my family, to the best of my knowledge.  They areType 1 diabetes, Celiac disease, ulcerative colitis.


human_id: hu70552D
date: 2014-11-02 01:00:16
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  my daughter had her genome coded by 23andme.com and told me on her maternal side it was J2B1a  and I have rhNeg blood type B if that helps


human_id: hu1312FD
date: 2014-11-26 20:33:42
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I was born with a heart defect (a coarchtation of the aorta).  While I was the only person I know of in my family to have had this defect, heart disease is common on both sides of my family.


human_id: hu169AC5
date: 2014-12-01 11:15:15
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  The only thing of note is that I have several unrelated cancers in my family. Paternal Grandfather died of Melanoma, Paternal Uncle died of Colon Cancer and Father died of Head & Neck Cancer. Also if you are looking for a way to collect a sample from me, I am a research nurse and would be happy to sent out a tube of blood to you, just let me know what tube you would like it collected in.


human_id: hu9E4FA5
date: 2014-12-07 21:50:39
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  possible diagnosis of Ehlers-Danlos, hypermobility / vacsular type (self) ... currently a working diagnosis


human_id: hu4D62E5
date: 2014-12-11 11:38:09
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  My dad is fully racially Italian.  My mom is mixed English, Irish, French, German, Scottish, Welsh, and Native American (in equal parts, but two parts Irish).


human_id: hu163E88
date: 2014-12-31 23:34:23
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have Oculocutaneous Albinism type OCA1, Autoimmune Progesterone Dermatitis, Ehlers-Danlos syndrome, Long QT syndrome, Polycystic Ovarian Syndrome, and a congenital septate uterus.


human_id: hu2B76CC
date: 2015-02-01 16:43:54
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Maternal lineage is of Polish descent. (diabetes common among ancestors)\n\nPaternal lineage is of Scottish descent.  (prostate cancer common among ancestors)


human_id: huE44F41
date: 2015-02-01 18:29:11
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  1:  Superior Canal Dehiscince syndrome: had a crainiotomy in 2010 to repair the bone that deteriorated on the right side between my brain and inner-ear. I have the same problem on my left side.\n2: Connective tissue disorder believed to be a form of Ehlers Danlos syndrome.


human_id: huE7271F
date: 2015-02-06 11:37:18
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Sensory modulation disorder\nFood Sensitivities (dairy, soy, blueberries, almonds)\nEmotional Sensitivity\n\n


human_id: hu50B3A1
date: 2015-02-14 04:08:25
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  759.89 Congenital hemihypertrophy, diagnosed 1/2015 @ University of Arizona Medical Center\nAnatomically shorter right leg, pelvic tilt, muscle atrophy of right leg\n\nFibromyalgia diagnosed 11/2014 @ UAMC\n\n


human_id: huF421B2
date: 2015-02-22 15:54:04
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  These may not be severe genetic disease or rare genetic trait.\none copy of Leiden V Factor\nelevated homocystine\nelevated triglycerides (mother's was diagnosed at the level of 3000+)\nelevated cholesterol, low HDL, high LDL with Xanthomas\nhypersensitive to betablockers\nhypersensitive to metals including silver\n \n\n


human_id: hu692C09
date: 2015-02-26 23:31:27
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Grandfather with Huntingtons Corea\nFather with ALS\nSister with Type I diabetes\nMaternal Grandmother with Charcot-Marie-Tooth\nHave high-fat/red meat/pork diet but have zero (0) % arterial plaque!  I would like to find out why and see if can help others.


human_id: hu918363
date: 2015-04-02 21:17:20
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have a very rare genotype, which is seen in 0% of the CEU population. I am homozygous A;A (T;T) for Rs1913474: \n\nRs1913474: [PMID 18636124OA-icon.png] Polymorphisms in the estrogen receptor 1 and vitamin C and matrix metalloproteinase gene families are associated with susceptibility to lymphoma.\n\nI have had a LOT of dental work in my day, including many fillings, crowns and bridgework with metal pins, and suspect I have a low grade lymphoma in my jawbone. I have only been diagnosed with Chronic Fatigue Syndrome (CFS) by my medical doctors, which I have had for over 15 years now. \n\nI am curious as to whether or not this genotype is linked to CFS.


human_id: huD0D2F9
date: 2015-04-04 23:50:30
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I do not have an addictive personality.\nI am susceptible to rheumatoid arthritis.\nI am unusually susceptible to basal cell carcinoma.\nI score in the top two percentile of standardized IQ tests.\n


human_id: hu04260F
date: 2015-04-06 19:35:28
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I'm not sure. I developed thyroid cancer before 18, which might indicate a genetic predisposition to that, but I don't know about a familial history of thyroid problems.


human_id: hu40C6BA
date: 2015-04-30 14:40:20
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Hereditary Dark Circles, like black eyes; elevated bilirubin, lactose intolerance, fibroids, dysmenorrhea, anemia, allergies, elevated ANA


human_id: hu5E3021
date: 2015-05-01 16:58:45
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have Amyotrophic Lateral Sclerosis (ALS).  Even in my case don't have any family members that are or have been affected with this disease, there are some genes, such as C9ORF72,  that have been found to have some correlation with what is considered "sporadic" ALS. Sporadic ALS may be promoted or even caused by a multi-gene factor coupled perhaps with some other trigger. For this reason,  whole genome analysis of many sporadic ALS patients may help discover new genetic variants that may contribute to the development of this disease.


human_id: hu0EB0AC
date: 2015-05-29 05:07:54
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  >My mitochondria haplogroup sequenced by genwhiz last year, sampled and PCRed by myself in a lab course in my college\nNNNNNNNNNNNNCTATTCTCTGTTCTTTCATGGGGAAGCAGATTTGGGTACCACCCAAGTATTGACTCACCCATCAACAA\nCCGCTATGTATTTCGTACATTACTGCCAGCCACCATGAATATTGTACGGTACCATAAATACTTGACCACCTGTAGTACAT\nAAAAACCCAATCCACATCAAAACCCCCTCCCCATGCTTACAAGCAAGTACAGCAATCAACCTTCAACTATCACACATCAA\nCTGCAACTCCAAAGCCACCCCTCACCCACTAGGATACCAACAAACCTACCCACCCTTAACAGTACATAGTACATAAAGCC\nATCTACCGTACATAGCACATTACAGTCAAATCCCTTCTCGCCCCCATGGATGACCCCCCTCAGATAGGGGTCCCTTGACC\nANNNCCATCCNN


human_id: huDE3564
date: 2015-06-11 14:05:59
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Ehlers Danlos Syndrome, Hashimoto Thyroiditis, Dilated Cardiomyopathy and many of conditions caused by the three listed above.


human_id: huB69975
date: 2015-07-05 16:46:47
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  clinodactyly\nvisual snow \ntinnitus \ndandruff \nalzheimer's disease \nparkinson's disease \nurinary incontinence \n\n\n


human_id: huEBE457
date: 2015-07-14 22:51:21
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have no genetic diseases or rare genetic traits, but I was born in 1994, not 1992. I only picked 1992 because that was the latest year available.


human_id: huC11596
date: 2015-08-09 21:52:57
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Familial dominant neuromuscular disorder - not yet identified - neurologist is about to ship me off to UMD and from there, if no answers, to NIH (which is where previous neuro tried to send me immediately).  \n\nMyotonia + myalgia from early childhood, worsened by tiredness, cold, hunger (particularly lack of refined carbs/sugar), and ESPECIALLY inactivity.  Made better by moderate exercise, but with a rebound effect after too much exercise.  Also improved with heat and massage (but not stretching).  Very low lactate threshold.  Hyperreflexia in me, but according to mother, grandmother (with same condition) had complete areflexia from her teens.  Mother and grandmother both have/had pronounced peripheral neuropathy, and my last workup found some, too.  I've had parasthesia, fasculation, and neuralgia (the last I believe from nerve impingement due to chronic myotonia), but these largely resolved with large amounts of moderate exercise.  MRI was clean.  Action tremor from teenage years at least (others noticed and commented first).  No impact on intelligence with age (mother scored in 99.99th %ile on the GRE at 50, as I did at 22, back when it was actually hard).\n\nNo cardiac or smooth muscle abnormalities at all.\n\nA small mutation of my SCN1A gene was found of unknown importance.  Other than that, a channelopathy screening came up clean.  This neuro isn't sold on the channelopathy angle and suspects something more dastardly, but he saw me when my conditions were at their worst--which, as I said above, I suspect are largely caused by irritation or impingement on the nerves by the badly behaved voluntary muscles, NOT because of some kind of nerve disorder, CNS or otherwise.  Another doctor's pet theory is a mitochondrial metabolic disorder, which I find pretty unlikely given its dominant inheritance.


human_id: hu98FFC6
date: 2015-08-13 00:37:51
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Hashimoto's Thyroiditis - Positive identification in early 30's. Older sister was diagnosed and suggested I test for it. TSH level have consistently been the low end of normal. Do not take any thyroid medication. Lowest levels were correlated with a strict gluten-free diet that I did for a year. I have had negative results for gluten sensitivity. I do not strictly follow a GF diet at this time.\n\nPossible diagnosis of "Undifferentiated Spondylo-anthropathy" by an osteopathic rheumatologist. Originally sought diagnosis from  DO related to inflamed Achilles Tendons in late 30's. Test have been negative for B27, Lupus, RA, Lyme, etc., yet C-Reactive Protein is consistently elevated.


human_id: huD09050
date: 2015-08-29 11:41:07
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I carry polydactyly gene (I never had the extra digits, but my father and my son both did).\nI have extremely small feet (probably < .01 % of men my height have feet as small as mine).\nExtreme susceptibility to motion sickness.


human_id: hu6D1115
date: 2015-08-29 14:50:27
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  not so rare but also not well understood MTHFR C677T heterozygous plus some other mutations in genes/SNPS in the methylation cycle


human_id: hu62F5A1
date: 2015-09-10 12:42:49
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  My eye doctor tells me I have tigroid fundum, a trait he rarely sees and many people in the Middle East have this trait.


human_id: hu10771F
date: 2015-09-17 17:29:36
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  (I just want to specify that my maternal grand-parents are from Spain - but I checked "White" - not "Hispanic" as, for me, this refers to South America...  let me know if I should correct this - thank you)


human_id: huC0FD53
date: 2015-09-23 08:14:21
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have relapsing remitting multiple sclerosis.  I'm not sure if you'd consider that 'severe' or primarily genetic, but I'll complete the disease surveys as appropriate.  Thanks for making this site and project available - it looks quite interesting and promising!


human_id: huB10361
date: 2015-09-30 18:38:01
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  some kind of connective tissue disorder, most likely Ehlers-Danlos of some type, with mitochondrial disease symptom overlap, severe Gastroparesis, history of early family deaths due to aneurysms etc. (maternal side), early heart attacks, cancers- also have a polymorphism on POLG (on 23andme), and for classic EDS (on 23andme).  I also have metabolic acidosis with hypokalemia, and many polymorphisms on the RYR1 gene.


human_id: hu6157D1
date: 2015-10-20 12:16:50
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  nothing severe.  also, my paternal grandfather by record (German), is potentially not biologically related to my father. It would not be surprising to us.


human_id: hu7FC773
date: 2015-11-01 18:43:16
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Have tested positive for Sweat Chloride/Sweat test.  Positive results for CF. Not diagnosed as of yet. \nSevere Chronic Pain, Bone Pain with Deterioration, seems to be genetic. \nStomach Issues, Chronic throughout family History.  For Crohns, IBS, IBD, Colitis, Gastroenteritis, Chronic Pancrititis. Seems to be a genetic Factor.


human_id: huA84F63
date: 2015-11-22 13:18:09
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  a rare mutation in a SNP linked to Ehlers-Danlos that codes for vascular integrity, specifically the integrity of the aorta.


human_id: huEFD66A
date: 2015-11-30 13:52:35
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have a half-uncle who died of Creutzfeldt-Jakob, unknown if it's the genetic kind. I have Ehlers-Danlos Syndrome.


human_id: hu4F0DF0
date: 2015-12-08 03:38:11
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  My pinky fingers are crooked,curved in,. There bone stops half way up. It is just cartilage. My mother and Twp daughters also have it.


human_id: hu4F0DF0
date: 2015-12-08 03:48:27
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Crooked pinkies. After the middle joint I have no cartilage. My mother, her uncle, and my two daughters also have it, but mine is more severe.


human_id: huD2F14E
date: 2015-12-12 02:49:52
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  HLA-B27 \nHigh positive ANA titer centromere pattern\nAuto immune disease that effects my upper trunk-necrotic lesions\n\n


human_id: hu15CCF3
date: 2015-12-29 09:59:27
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  My paternal grandmother and her daughter had/have hypothyroidism as do I. The daughter does not have the same father as my father does.


human_id: hu522703
date: 2015-12-29 19:47:22
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  None that I know of.My doctor said to me once that my heart was on the opposite side of most peoples, but other than that there is nothing else I know of that could be genetic.


human_id: hu6BF6F9
date: 2016-01-03 18:15:44
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  My paternal grandfather died at age 40 of "kidney failure".  My father was chronically depressed.  My grandfather died prior to 1915 when suicide was not an open subject.


human_id: hu70552D
date: 2016-01-05 20:52:33
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Neg B bloodtype\n\nHad some genetic testing done for medical pharmaceutical diagnostics at GeneSight, Had some genetic mutations/variants that they stated in the reported as: \n"The following rare genetic variants have not been observed by the Assurex  Health, Inc. laboratory: CYP1A2 125C>G, 5166G>A, 558C>A; CYP2C19 *7 "  \nDon't know if that may be of interest to you.  I'm very interested to know more about my blueprint of course. Thanks.


human_id: hu0739F4
date: 2016-01-07 12:27:07
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Potential carrier for either AIPorphyria or VPorphyria. Daughter shows positive for both HMBS and PPOX genes in line by line analysis of raw data provided by 23andMe, December 2016.


human_id: hu88F5BD
date: 2016-01-07 14:41:41
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Diagnosed with acute porphyria 1984, University of Washington Medical Center. Records seized by Group Health insurance company. No records retained by me or by the university.\n\nFather and Sister both also test positive for AIP.


human_id: huD70430
date: 2016-02-04 16:47:45
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have been diagnosed with Multiple Sclerosis. I also have a 17 year old son who was born with Down Syndrome.


human_id: hu8C9ABA
date: 2016-02-10 00:04:31
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Genetic spinal stenosis.  Of 6 children in my family 5 of us have this condition and have had multiple related surgeries.


human_id: huF9F779
date: 2016-02-17 21:38:02
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Nothing that we know of yet.  However, myself, my brother, my father, and my uncle (father's brother) all exhibit Attention Deficient Disorder, which I am currently taking medication for.  I am also being screened for Asperger's via the DSM-5, but results are not yet known.


human_id: huC70CEE
date: 2016-03-18 17:48:31
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Ethnicity of paternal grandfather:  Scotch-Irish, German, English\nEthnicity of paternal grandmother:  English and German\nEthnicity of maternal grandfather: English and Scotch-Irish\nEthnicity of maternal grandmother:  English\n\nThe only people who are ethnic Americans are American Indians!  What are you thinking asking people where their grandparents were born can tell you?


human_id: hu892206
date: 2016-03-20 14:40:45
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have Synovitis Acne Pustulosis Hyperostosis Osteitis (SAPHO), which is a rare syndrome. It is unclear if it is genetic or not.


human_id: hu96959E
date: 2016-04-11 17:50:57
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Grave's Disease,  Hashimoto's thyroiditis, SLE (myself and cousin), Rheumatoid Arthritis (myself, sister, cousins have), father has hemochromatosis and do not know if I have the markers, my son does have 1 marker


human_id: hu01EECF
date: 2016-04-12 16:51:39
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have Reynaud's disease. Seems to be on my maternal side, a maternal Aunt has been diagnosed as well as a maternal cousin.


human_id: huE9B080
date: 2016-04-24 20:09:04
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Late Adult Onset Partial Biotinidase Deficiency.\n(Unverified. Learned from PGP data, took Biotin with next day significant improvements in energy levels.)\n\nFemoroacetabular Impingement (FAI). Both Cam and Pincer type.


human_id: huE6E6C9
date: 2016-04-26 14:50:42
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Ehlers Danlos Syndrome type III\nRare mitochondrial variants: TRNC nt# 5825 heteroplastmy 9%, CYTB nt#15175 c.429T>C heteroplasmy 12%.\nPostural orthostatic tachycardia syndrome\nneurocardiogenic syncope\nmigraines\n


human_id: hu3269F6
date: 2016-05-03 16:00:27
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have a bicuspid aortic valve, which appears to be familial. My paternal grandfather had a bicuspid aortic valve and my brother has slight aortic abnormalities (but does not qualify as pathogenic).


human_id: huFB87DF
date: 2016-05-08 15:35:13
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have been told I am a carrier of hemachromatosis. All 4 of my sons tested positive for 1 of the mutations. 2 have the active disease, requiring phlebotomies. My husband who is 100% "Polish" decent, is also a carrier.


human_id: hu3E6FA7
date: 2016-05-31 18:27:22
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  SDHB germline mutation C189F\nFather died of paraganglioma (a rare cancer)\nAunt (his only sibling) died of paraganglioma\nI inherited the mutation and have SDHB deficient Gist Cancer


human_id: huCED936
date: 2016-06-23 09:51:37
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  yes Ihave lynch syndrome diagnosed by the v.a. and they tod me you guys will never give me the test results of my own and that i was being used >? somehow? hope that isnt truer and just takes a long time, also filling out this form I could not find either scotland or england listed as countries???


human_id: hu531522
date: 2016-07-07 14:09:32
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  My mother's family has Alport's syndrome.  My mother does not display symptoms and neither do I.  But at least two of her sisters have severe version of the disease and it's possible at least one of her brothers did.


human_id: huD23DC7
date: 2016-07-19 22:04:47
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have Polycystic Ovarian Disease and a possible unknown genetic mutation (paternal grandfather and his brother had breast cancer but grandpa was BRCA negative)


human_id: hu4EEA9B
date: 2016-07-27 11:12:04
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I don't have any medical conditions.  I used to suffer from severe alcoholism, but ended that in early 2011.  My family, however, does have some history of medical conditions.  On my father's side, there have been several heart-related issues.  They have seemed to not be as prevalant since diets have changed in a few generations of relatives.  On my mother's side, my uncle, first cousin, and a farther back relative have all suffered some sort of schizo spectrum disorder.  I know personally that my first cousin's schizophrenia was triggered by him using methamphetamine and various other drugs.  I thought I was going to end up the same because of my alcoholism and family genetics, but have absolutely no paranoia or any related symptoms.


human_id: hu4EEA9B
date: 2016-07-29 19:27:14
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  My family has very diverse ethnicities.  I have tried to trace this down since I was a child, and have recently compared my DNA with several populations.  If you would like the results to this data, I'll be glad to email them.  My ethnic profile is primarily Western European, with a lot of Mediterranean.  I have been told that I have a lot of Greco-Italian genes, but that I am mostly a Euro-mutt.  I also have some Native American ethnicity.  My DNA analyses have shown roughly 9% likelihood of Middle/Near Eastern genetics from the SNP comparisons, and is most likely due to the amount of relatives I've had from the Mediterranean area (most likely mingled with Middle Eastern Jewish populations).  From my best guess, my ancestry runs through every population except African and East Asian ethnic groups.


human_id: huFB87DF
date: 2016-08-02 00:48:34
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  hereditary hemachromatosis carrier, as is my husband. All four sons have mutation. Two of them require phlebotomies.\n\nOne son had ablation of Mayhaim fibers.


human_id: hu4623CD
date: 2016-08-13 11:53:37
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  My maternal great grandmother had a large port wine stain on her head. I have a small light one on the back of my neck.


human_id: huDD5D00
date: 2016-09-05 11:35:00
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Bipolar Disorder II. ADD. I don't go through withdrawals from medications (such as opiates which I took for a long time because of a broken leg or benzodiazapines). My father and uncle were heavy drinkers and quit but never went through the DTs or needed medical assistance. My tolerance for medication seems to increase faster than normal people and it seems impossible to get it to go back to normal no matter how long I've been off the meds. I have an addictive personality, low-self esteem, have self-medicated in the past. Addiction (specifically alcoholism) has run in my family since, at least, before the Civil War as noted by great-great-great (?) grandfather Dr. Jacob Perry Welch who wrote a journal for posterity. I also suffer from insufferable anxiety.


human_id: hu297A5D
date: 2016-09-19 04:40:34
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have had various mental health diagnoses: Diagnosed with ADHD at age 5, pervasive developmental disorder NOS (now autism spectrum disorder) at 6, conduct disorder by 9, Asperger's disorder at 13 (now autism spectrum disorder), schizotypal personality disorder at 14 (with an accompanying psychotic break), and major depression at 32.\n\nWas diagnosed with macrocephaly as a child; today, my head is merely large, and appears to be strongly brachycephalic but within normal variation.


human_id: hu48D5DB
date: 2016-09-27 19:02:00
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Diagnosed clinically with Glutaric Acidemia type 2 (GA2, AKA Multiple Acyl-CoA Dehydrogenase Deficiency, MADD) based on repeated sets of biochemical testing (concentrations of plasma acylcarnitines of various chain lengths were significantly elevated). Hx elevated NH3 & CK; carnitine deficiency; acute renal failure; lactic acidosis; encephalopathy; hydrocephalus; dysautonomia; and connective tissue disorder. Targeted genetic testing for ETFA, ETFB, and ETFDH negative. WGS pending.


human_id: hu7BBD72
date: 2016-10-07 15:51:59
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  VARIANT PRESENT ON GENE RP1L1\nAUTOSOMAL DOMINANT PATTERN\nTO ME THRU MY FATHER, FROM HIS MOTHER\nOCCULT MACULAR DYSTROPHY\nNOTED ON VISION AND HEARING SURVEY


human_id: hu4F2901
date: 2016-10-28 07:29:37
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  My mother has a cleft chin, asthma, COPD, and osteoporosis. Her half sister has Parkinson's Disease. I have been diagnosed with Multiple Sclerosis (but do not have genes that predispose me; as I was told from another study). I have also been told that I could have a negative reaction if I take Warfarin and a predisposition for asthma. I believe that I could pass on to my children but do not recall what that was.


human_id: hu11A662
date: 2016-12-07 23:07:36
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Enlarged right lateral ventricle of the brain- this has been attributed to diagnosis similar to NVLD.


human_id: huC9C933
date: 2016-12-11 22:31:15
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Russian Mennonite on mother's side, Swiss Mennonite on father's side\nOCD\nNarcolepsy\nPoland's Syndrome (left side)


human_id: hu136241
date: 2016-12-27 01:06:53
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Present from birth: Large linear nevus sebaceous on front left side of scalp\n\nPresent from < 6 months: Undiagnosed seizures


human_id: huFE1782
date: 2017-01-18 01:05:42
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  father has metabolic syndrome, high blood pressure, heart disease, diabetes, I run very low temperatures, allergic to the flu vaccine, I have ehlers danloes hyper mobility, and reynauds and perioidic paralysis. \n\n


human_id: huB06CDB
date: 2017-02-14 12:52:38
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  heterochromia iridum\nTested for the CCR5 (negative)\nDesire testing for the SOST gene (never a broken bone /have dense bones)\nDesire testing for HLA gene(s) because of my fibromyalgia and depression \n


human_id: huB74692
date: 2017-03-11 11:18:41
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Duypetrenne's  (spelling?)\nbrother paranoid schizophrenic\ndaughter CFIDS/SEID or reasonable facsimile thereof


human_id: hu70B72E
date: 2017-03-11 22:25:53
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have hypothyroidism which a maternal uncle also had, my parents both had goiters. My mother had a baby before me DOB 6/13/54 which died just a few days after birth from erythroblastoma - she was a 'blue baby' at a time when there was no treatment for Rh incompatible babies. From what I've read each subsequent pregnancy the risk increases for this condition, yet I was born healthy (& this was before they developed treatments which now essentially eliminate such fatal events). However, between the ages of 25-30 I was besieged by a number of health issues beginning w/psoriasis, psoriatic arthritis, fibromyalgia then hypothyroidism & have always wondered if the Rh factor incompatibiity somehow made me more vulnerable to these chronic health issues at a relatively young age. More recently I was diagnosed w/osteoporosis & neuropathy. Though my mother had neuropathy hers was related to type 2 diabetes (1 of her bros. also had type 2 diabetes) however I'm regularly tested for this & so far have been negative. And though my mother, her mother & myself have all been small boned, I'm not aware that they had osteoarthritis. Note: when my parents died I had specimens frozen in case their DNA could be useful in the future in relationship to my own health.


human_id: huE9B080
date: 2017-04-06 23:48:18
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Experienced noticeable improvements taking Biotin 5,000 mcg/day after learning of BTD-D444H carrier status. Later tested negative for Biotinidase deficiency in bloodwork. \nFemoroacetabular Impingement (FAI). Both Cam and Pincer type.


human_id: huD0D2F9
date: 2017-04-21 23:21:26
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I am not addictive to addictable substances. The trait was passed paternally if, in fact, it is genetic at all.\n\nI am 68 years of age.  While my father passed at 71, his father lived to the age of  100 despite drinking and smoking all his life. My Great Grandfather on the pater side was also long-lived.  My maternal ancestors seem to have expired in their 70s, as I expect to do.


human_id: hu3D9348
date: 2017-04-22 02:04:41
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Ehlers Danlos Syndrome - Hypermobile Type\n\nAutoimmune/Hashimoto’s Thyroiditis \n\nIdiopathic Intracranial Hypertension \n\nLupus/Sjogren's Syndrome


human_id: hu0C9503
date: 2017-04-24 15:12:24
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I wouldn't call it rare, but members of my family from my father's side are all missing very specific teeth and this trait seems to be passed on to each generation, but only affects the first born children that happen to be of the opposite sex than the carrier parent, i.e. a male with the trait happens to have a female firstborn child whom also carries the trait.


human_id: hu9764AA
date: 2017-05-26 18:40:47
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  White blonde hair (tow-head) and light green eyes. \n\nWas mauled by a bear, fought it off and drove myself down a mountain for help with my face hanging off.  At age 58/F 5'1" 107#  (which is to say, an ornery type old lady).


human_id: hu52B7E5
date: 2017-08-03 11:01:29
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  My maternal great-grandmother, my mother, my maternal aunt, and I were all diagnosed with pre-menopausal breast cancer. My great-grandmother was 43, my mother was 43, my aunt was 48, and I was 39. My aunt had a recurrence again at age 70-something. I have been tested for about 17 different known mutations associated with breast cancer, but none have been identified.


human_id: hu5D06D5
date: 2017-08-29 16:11:06
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Ehlers-Danlos Hypermobile (symptomatic diagnosis)\nEhlers-Danlos Vascular (suspected, not yet diagnosed)\nHemochromatosis (working on getting diagnosis)\nDenisovan (GenoGraphic results)\nNeanderthal (GenoGraphic results)


human_id: hu94876C
date: 2017-09-11 13:34:33
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I don't have any genetic diseases or rare traits.  \n\nMy son was diagnosed with Pilomyxoid Astrocytoma at four months, but not sure if it is relevant.


human_id: hu566097
date: 2017-09-22 10:43:11
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  My skin turns purple-red molted coloring, if the temperature around me drops below 74 degrees. My dermatologist said it was a genetic condition, and she asked me, at what temperature, does my skin start to change colors. I am a white female.  \n     When I was tested with the National Geographic Geno 2 test, I downloaded my raw DNA. I also found out that I am Denisovan 2.4%, Neanderthal 2.3%, 2.4% Ambiguous, and the rest is Modern Human. \n     I was an RH baby born in 1964. I was told that I spent the first 6 months of my life in Children's Hospital, Pittsburgh, Pa., because my mom's and dad's blood was fighting inside of me. One of the reasons I lived, was because, my dad's brother was Dr. James K Greenbaum, and he was a really good Pediatrics doctor from, Kittanning, Pa., who just passed in 2013.


human_id: hu241563
date: 2017-10-07 21:53:59
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Early stage HFE hereditary hemochromatosis: discovered after an iron deficiency panel yielded a ferritin value of 461 ng/ml (standard range 20 - 380 ng/ml).  Subsequent genetic testing showed heterozygous for the HFE H63D mutation and heterozygous for the HFE S65C mutation (compound heterozygous H63D/S65C) that may cause a greater than normal intestinal absorption of dietary iron.  Increased iron may result in damage to liver and other organs but an MRI showed that there was not any noticeable build-up of iron in the liver.


human_id: hu241563
date: 2017-10-07 22:09:04
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Heterozygous for the HFE H63D variant and heterozygous for the HFE S65C variant (compound heterozygous H63D/S65C) that may cause a greater than normal intestinal absorption of dietary iron (HFE hereditary hemochromatosis).


human_id: hu7FF48E
date: 2017-10-11 22:28:25
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have Narcolepsy with Cataplexy \n         as well as showing most if not all of the various side issues that ride along with it.


human_id: hu691345
date: 2017-10-22 15:40:56
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  AMPD1 deficiency (snp rs17602729(T;T)\n\nTelomerase challenge? Interesting because of pulmonary "issues", asbestiosis, COPD at relatively young ages in our family, maternal especially. Have interesting snp in TERT: rs2736100(T;T)\n\nApparently at very increased risk for macular degeneration (multiple snps) and my paternal grandmother was severely affected. rs10490924(T;T)\nrs4151667(A;T)\nrs5888(C;T)\n\nHave had lots of inflammatory arthritic and degenerative challenges, including Hashimoto's hyper/hypo-thyroidism, elevated ANA (resolving now) and nerve damage in lumbar spine from herniated disc material that would have normally been resolved/resorbed but, my neurosurgeon informed me that my body had calcified the material which then rebroke and damaged the nerve. Several doctors have told me that small cysts had calcified and that this was not typical. I don't know if this is something that may have significance but I suspect it does. Particularly if these calcifications could also occur more frequently than average in inflammatory areas of cardiovascular and brain ++\n\nThank you!


human_id: hu691345
date: 2017-11-29 15:41:21
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  AMPD1 deficiency; TERT variant which is linked to impaired telomere repair, pulmonary fibrosis and accelerated aging. Lots of autoimmune variants, CFH, FGFR4 and more. Lots of inflammatory and autoimmune conditions plus pulmonary issues in our family. Likely heart arrhythmia with lots of A-fib and ventricular dysrhythmia -- even at young ages, at least on my paternal side and for myself. Lots of fainting spells with any intraabdominal pressure or pain --- since teenage years -- hard to figure out -- elevated adenosine due to AMPD1 issue?  Brugada genes partially affecting?


human_id: hu85F3ED
date: 2018-02-01 20:43:53
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  Document info\nResult type: MRI Chest wo then w Contrast\nResult date: Jul 15, 2015, 10:27 a.m.\nResult status: authenticated\nPerformed by: Jason Ford\nVerified by: Jason Ford\nModified by: Jason Ford\nAccession number: 00000MR20150036596\nMRI Chest wo then w Contrast\nPatient: Greis, Kurt D DOB: Feb 23, 1954\nReport\nEXAMINATION: MRI Chest with and without intravenous Contrast\n\nCOMPARISON: Ultrasound upper back dated 6/17/2015\n\nRELEVANT CLINICAL INFORMATION: Patient with soft, palpable mass on\nthe right upper back, inferior to the scapula. As per patient, this\nhas been present for 6-7 years, however, has grown in size and is now\npainful when laying on a hard surface.\n\nTECHNIQUE: Multiple routine MR pulse sequences were obtained of the\nchest before and after the use of IV contrast. 15 mL Magnevist was\nadministered intravenously without adverse event.\n\nSEDATION: NONE\n\nFINDINGS:\nThe localizer images were reviewed. Limited evaluation of the right\nlung, thoracic spine, spinal canal and aorta demonstrate no acute\nchanges. Small bilateral cysts are noted within the neuroforamina,\nimage 32 of series 8 with additional small cyst noted within the\nright neural foraminal canal, image 20, involving mid to lower\nthoracic vertebral bodies, most consistent with perineural root \nsleeve cysts. There is no associated contrast enhancement.\n\nAlong the right upper back, there is redemonstration of a lobular,\nfat signal mass with multiple thin internal septations. Mass extends\nalong the margins of the right trapezoid fascia, inferolaterally to\nthe level of the right latissimus dorsi. This is difficult to measure\ngiven its extent along the back wall, however, when measured in\ncoronal and axial sequences, this measures up to 15 x 6.8 x 2.0 cm in\nits greatest dimensions. There is mildly increased signal within the\nsuperior lateral aspect of the fatty components of the mass on both\nprecontrast and postcontrast sequences of uncertain significance. No\nenhancing soft tissue element is identified. No discrete nodular or\nsolid-appearing component is identified. There is no cystic\ncomponent. There is a moderate-sized vessel coursing through the mass\nand extending superficially near the skin surface.\n\nIMPRESSION:\nMRI CHEST WITHOUT AND WITH IV CONTRAST.\n1. A 15 x 6.8 x 2.0 cm probable lipoma with somewhat atypical\nfeatures. No focus of soft tissue enhancement identified to suggest\nliposarcoma. However, given history of interval enlargement and\ndevelopment of pain, recommend surgical consult.\n\nNOTE: Results communication documented in primordial.\n\nThank you for the opportunity to assist in the care of your patient.\nIf there are any questions about this examination, please page Dr.\nJason Ford fellowship trained, board certified radiologist at\n317-367-7326.\n\nElectronically Signed by: Ford, Jason\nDictated on: 7/15/2015 10:36 AM


human_id: hu6368DD
date: 2018-02-11 06:28:48
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  VERY HIGHLY suspect 2q32 2q33.1 micro/deletion syndrome. Had 3 orthognathic procedures due to sudden abnormal/face jaw growth in mid-teens. Jaws/face/teeth have shifted and warped and continue to do so. I also have/had almost every other symptom of those disorder(s).\n\nSuspect possible Hemochromatosis but have never been tested. I am a carrier of one C282Y and one H63D.


human_id: huEAC017
date: 2018-03-12 23:51:31
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I am missing my 5th lumbar vertebra. I have bone islands in my hips. I and my two brothers have severe arthritis, RA in one brother, psoriatic in my other brother, and I have degenerative osteoarthritis.  My thyroid was removed in 2011 due to countless (literally) bilateral cysts and nodules.


human_id: huFEDD4D
date: 2018-03-22 03:52:25
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have a blood clotting disorder called Protein S Deficiency. It is supposedly inherited but my mother tests positive for a different disorder known as Antithrombin III Deficiency.


human_id: hu50CF0E
date: 2018-05-11 19:38:36
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I am a carrier for Usher Syndrome (Type 2), through my father.\n\nI also am a carrier for Cystic Fibrosis.


human_id: huD7FF22
date: 2018-05-25 02:49:00
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  I have multiple autoimuune disorders that they just can not figure out. Been trying since 2014. I have hypothyroid, i had psos before hysterectomy, had 3 back surgeries, chronic sphenoid disease, they say i have syndrome of inappropriate antidiuretic hormone, Barrett’s esophagus. I am a medical mystery at this point. Hypertension, high cholesterol. I am not overweight.


human_id: huB173FD
date: 2018-06-16 04:53:10
phenotype_category:
[cell repeats an earlier one in this file: 136 characters]

phenotype:
  23&me says I have an increased risk of Parkinson's Disease. They detected the G2019S variant in the LRRK2 gene. My son has the same result. I am not symptomatic and have not been diagnosed with the disease as of yet.


human_id: huED0F40
date: 2012-10-12 00:41:16
phenotype_category: Blood:other
phenotype:
  Undiagnosed/Subclinical  for Pernicious Anemia but show some signs; Folate & Iron Levels have always been good. Father had years of low B12 and Vitamin D3 Deficiencies


human_id: hu60180F
date: 2012-10-25 22:07:19
phenotype_category: Blood:other
phenotype:
  have an intermittent defect that cause severe bruses, was worked up at blood center of wisconsin, I can find results if you want them


human_id: hu64A49C
date: 2016-06-28 17:47:47
phenotype_category: Blood:other
phenotype:
  was told I was anemic during pregnancy and several times during my life, but no idea of type of anemia or cause


human_id: hu48D5DB
date: 2016-09-27 21:03:12
phenotype_category: Blood:other
phenotype:
  macrocytic anemia & pancytopenia, folate & carnitine deficiency in association w/ metabolic crisis and probably Glutaric acidemia type 2. Both mother and maternal grandfather have IgM Kappa. Mo dx w/ smoldering myeloma. Grandfa had chronic lymphocytic leukemia


human_id: hu48D5DB
date: 2016-09-27 21:05:22
phenotype_category: Blood:other
phenotype:
  macrocytic anemia & pancytopenia w/ probably GA2. Mo and fa both have IgM Kappa spike, mo w/ smouldering myeloma and grandfa w/ chronic lymphocytic leukemia


human_id: hu7D3329
date: 2014-03-03 19:18:39
phenotype_category: Cancers:other
phenotype:
  Borderline ovarian tumor (had "suspicious" cells and was considered "pre-cancerous" and "dangerous."  Doctors actually did not agree about what borderline means and whether it is or is not a stage of cancer


human_id: huC51695
date: 2014-08-27 14:28:16
phenotype_category: Cancers:other
phenotype:
  Have had precancerous changes to the cervix removed via freezing during colposcopy, probable infection from HPV identified as cause.


human_id: hu98FFC6
date: 2015-08-13 00:51:55
phenotype_category: Cancers:other
phenotype:
  As yet, no indications for cancer though my mother died at age 52 from Breast Cancer that had metastasized. Her death resulted from Cancer of the pleural cavity. Breast cancer diagnosed at age 48; metastatic cancer diagnosed, death occurred 4 mo. after re-occurrance.


human_id: hu48D5DB
date: 2016-09-27 20:58:33
phenotype_category: Cancers:other
phenotype:
  Grandmo & great aunt w/ metastatic carcinoid, sister w/ SDHD mutation implicated in carcinoid, novel POLG deletion


human_id: hu36A9DD
date: 2017-08-12 10:29:14
phenotype_category: Cancers:other
phenotype:
  hypothyroidism, scoliosis, dyslexia, polydactyly, vasovagal syncope, lymphocytic microscopic colitis, osteoarthritis


human_id: hu691345
date: 2017-11-29 15:43:38
phenotype_category: Cancers:other
phenotype:
  severe endometriosis at young age along with large fibroid which apparently started in teen years, per doctors.


human_id: huED0F40
date: 2012-10-11 23:56:41
phenotype_category: Circulatory_System:other
phenotype:
  Myxomatous Degeneration of mitral valves without true prolapse; trace pulmonic insufficiency 09/18/2012 echocardiogram


human_id: hu60AB7C
date: 2013-01-12 21:20:54
phenotype_category: Circulatory_System:other
phenotype:
  My hemoroids were cured with sublingual Annhydrous Betaine 750mg upon awakening or at the onset of symptoms.  This also dropped my pulse 10 beats, and lowered my pressure by 10-20%.


human_id: huA099E6
date: 2013-03-04 10:14:54
phenotype_category: Circulatory_System:other
phenotype:
  father had heart valve replacement at age 72, as medium distance runner I never experienced any blood circulation issues


human_id: hu9745B5
date: 2014-03-27 00:10:05
phenotype_category: Circulatory_System:other
phenotype:
  Father's history includes, but not diagnosed in me: IHSS, congenital heart murmur, arrythmia, hemorrhoids, DVT, TIAs, Atrial Fibrulation, Pernicious Anemia, congestive heart failure,


human_id: huE34B72
date: 2014-12-11 12:40:57
phenotype_category: Circulatory_System:other
phenotype:
  I experience symptoms similar to Reynard's phenomenon; color changes in hands and feet, cold intolerance in hands and feet, and intermittent burning sensation in feet at night.


human_id: hu02A209
date: 2013-06-27 20:03:02
phenotype_category: Congenital_Traits_and_Anomalies:other
phenotype:
  Congenital heart defect is leaky / prolapsed mitral valve, hereditary on father's side; shared by my surviving half-brother, who had corrective surgery at birth (his twin had the same condition but died shortly after birth)


human_id: hu28391C
date: 2014-02-25 03:32:31
phenotype_category: Congenital_Traits_and_Anomalies:other
phenotype:
  As a child, I had a single tooth come in the top or roof of my mouth. It was removed and I've had no known complications from it.


human_id: hu3A1B15
date: 2014-04-12 10:58:19
phenotype_category: Congenital_Traits_and_Anomalies:other
phenotype:
  Had an "innocent murmur" as a child. But assume that doesn't count as "Congenital heart defect," so didn't check that box.


human_id: hu0C9503
date: 2014-07-24 01:57:12
phenotype_category: Congenital_Traits_and_Anomalies:other
phenotype:
  my father's side has a genetic quirk of being born without your incisors. My father's mother was born without incisors, my father and all his siblings were born without incisors, and their first born offpspring was born without incisors (incidentally all the first borns were of the opposite sex from the parent which passed on the trait)


human_id: hu36A9DD
date: 2017-08-12 11:41:15
phenotype_category: Congenital_Traits_and_Anomalies:other
phenotype:
  6th toe attached to last joint of great toe.  Removed at age 12 to prevent damage to great toe joint.


human_id: hu691345
date: 2017-11-29 15:51:28
phenotype_category: Congenital_Traits_and_Anomalies:other
phenotype:
  spinal bifida was not noted as covered by skin. But found during youth on a scoliosis xray, lumbar spine.


human_id: hu6368DD
date: 2018-02-11 06:51:07
phenotype_category: Congenital_Traits_and_Anomalies:other
phenotype:
  High and narrow upper palate and sudden, severe misgrowth of upper and lower jaws beginning in teens.


human_id: hu5DE8CD
date: 2012-10-13 12:30:43
phenotype_category: Digestive_System:other
phenotype:
  The roots on most of my baby teeth did not dissolve, and they were extracted whole to make room for new teeth around the age of 8.


human_id: huB220C0
date: 2013-01-30 14:27:18
phenotype_category: Digestive_System:other
phenotype:
  microscopic colitis, autoimmune disease, Hasimoto's, Sjogrens, Epilepsy, allergy (anaphylactic food allergies also)


human_id: huEAE6C8
date: 2013-04-26 17:12:11
phenotype_category: Digestive_System:other
phenotype:
  Fibromyalgia associated GI problems, as a teen had a lot of acid reflux, definitely no IBD- just had a colonoscopy


human_id: huBB058E
date: 2014-04-25 13:36:27
phenotype_category: Digestive_System:other
phenotype:
  Starting Nov2013 changed from constipation all my life to having soft stool the most recent past 6 months.


human_id: hu998A3D
date: 2014-08-08 18:32:58
phenotype_category: Digestive_System:other
phenotype:
  I was told several times I had symptoms of Crohn's, particularly since I had a perforated large intestine at 21 years of age. Small intestine was resectioned at 37.


human_id: hu462369
date: 2015-03-09 12:34:34
phenotype_category: Digestive_System:other
phenotype:
  Very strong stomach :) Thrown up only a couple of times in my life; would be good to study that trait!


human_id: hu98FFC6
date: 2015-08-13 01:21:34
phenotype_category: Digestive_System:other
phenotype:
  I am tongue-tie (ankyloglossia); Frenulum is still intact and I have never has speach or swallowing problems.


human_id: hu69BD84
date: 2015-10-06 09:28:21
phenotype_category: Digestive_System:other
phenotype:
  I have had hernia surgery, replaced my abdominal wall with mesh to keep my intestines on the side they belong on. I was told the birth weight of my children left holes in my abdominal wall and it needed to be replaced with mesh


human_id: huED93F6
date: 2015-11-20 13:04:20
phenotype_category: Digestive_System:other
phenotype:
  Collagenous colitis (brother had it, also), possible sarcoidosis of stomach lining, biopsy felt to be to superficial to uncover


human_id: hu512175
date: 2018-06-15 08:46:37
phenotype_category: Digestive_System:other
phenotype:
  I was diagnosed with pancreatitis several times after drinking alcohol starting at the age of 26/27 and finally ending up in the ICU of the local hospital at age 28/29. After being treated there for over two weeks with pancreatitis and fatty liver and excruciating pain the doctor discharged me as soon as I could eat solid food and go without the Dilaudid drip I was on for the pain.


human_id: huED0F40
date: 2012-10-12 00:23:35
phenotype_category: Endocrine_Metabolic_Nutritional_and_Immunity:other
phenotype:
  Low serum HDL 25-37 w/ Rx  Niaspan treatment;  Vitamin D3 Deficiency (25 or less readings during summer, w / a daily 2000 iU supplement )


human_id: hu8B6758
date: 2012-10-14 20:16:05
phenotype_category: Endocrine_Metabolic_Nutritional_and_Immunity:other
phenotype:
  Tested positive for thyroid antibodies although currently not testing in the normal range for hypothyroidism


human_id: huB10361
date: 2013-01-09 17:26:34
phenotype_category: Endocrine_Metabolic_Nutritional_and_Immunity:other
phenotype:
  lupus, low IgM (25) with abnormal response to vaccine titers, low IgG subclass 3, low C3-C4, metabolic acidosis, high LDL, homocysteine, elevated ACE at times, sometimes pos. ANA


human_id: hu04DF3C
date: 2013-01-12 18:22:22
phenotype_category: Endocrine_Metabolic_Nutritional_and_Immunity:other
phenotype:
  sensitive to milk - produces mucous and sore throat at times. much less sensitive to yogurt and many cheeses


human_id: hu4DB380
date: 2015-02-18 18:36:02
phenotype_category: Endocrine_Metabolic_Nutritional_and_Immunity:other
phenotype:
  Diabetes Insipidus, Secondary Hypogonadism, Chronic Fatiuge Syndrome, Multiple Chemical Sensitivities


human_id: hu4EEA9B
date: 2016-07-27 11:15:10
phenotype_category: Endocrine_Metabolic_Nutritional_and_Immunity:other
phenotype:
  I did have a medication that caused severe rapid weight gain, got high triglycerides, cholesterol, and blood pressure from that; got off the prescription, exercised, now healthy


human_id: hu48D5DB
date: 2016-09-27 21:00:37
phenotype_category: Endocrine_Metabolic_Nutritional_and_Immunity:other
phenotype:
  Elevated ALA & plasma tyrosine, phenylalanine, methionine; extreme adverse rx reactions + anemia. Tyrosinemia has been questioned


human_id: hu691345
date: 2017-11-29 15:46:22
phenotype_category: Endocrine_Metabolic_Nutritional_and_Immunity:other
phenotype:
  poor iron absorption, anemia, severe during pre-menopause, required years of IV iron supplementation until uterus removed. Father also was never able to donate blood due to anemia of no known cause. Paternal grandfather also had pernicious anemia.


human_id: huA099E6
date: 2013-03-04 10:18:03
phenotype_category: Genitourinary_Systems:other
phenotype:
  I had vasectomy done at age 24, sperms were normal at that time, no problems in any of these areas in my family


human_id: huBB058E
date: 2014-04-25 13:38:29
phenotype_category: Genitourinary_Systems:other
phenotype:
  Not diagnosed, but I suspect I've had kidney stones due to the painful experience passing them in urine.  My father has had many kidney stones after he turned 50 years old.


human_id: hu4DE348
date: 2012-11-03 01:25:59
phenotype_category: Musculoskeletal_System_and_Connective_Tissue:other
phenotype:
  recent ANA result 1:2560 speckled; awaiting further tests to determine type of connective-tissue disorder


human_id: hu5BD76A
date: 2012-12-10 18:32:12
phenotype_category: Musculoskeletal_System_and_Connective_Tissue:other
phenotype:
  I quit baseball because throwing caused pain in my throwing elbow in highschool, treated with aleive which helped.


human_id: huB10361
date: 2013-01-09 17:38:24
phenotype_category: Musculoskeletal_System_and_Connective_Tissue:other
phenotype:
  endplate sclerosis, bulge osteophyte complex, cranial instability/cervical hypermobility, stenosis, spondylosis, reversal of cervical lordosis, degenerative disc disease, multiple nerve root diverticula bilaterally throughout cervical, thoracic, and lumbar spine


human_id: hu60AB7C
date: 2013-01-12 21:28:31
phenotype_category: Musculoskeletal_System_and_Connective_Tissue:other
phenotype:
  There are a few areas in my back where the vertibrae have thinned (arthritis?).  MRIs and X-Rays are a part of my profile.  During sleep I ruptured two vertibral disks in my lumbar spine.


human_id: huBB058E
date: 2014-04-25 13:41:42
phenotype_category: Musculoskeletal_System_and_Connective_Tissue:other
phenotype:
  Carpal tunnel syndrome which I had a surgery on the inside of my right wrist to remove the "bump". My wrist is now fine, and I can play tennis.  The original carpal tunnel syndrome injury was the direct result of a very intense badminton game.


human_id: hu726FB4
date: 2014-09-11 20:55:04
phenotype_category: Musculoskeletal_System_and_Connective_Tissue:other
phenotype:
  right and left anterior cruciate ligament tear,  bilaterial meniscual tear, osteochondral defect right ankle


human_id: hu00D419
date: 2015-07-13 12:30:02
phenotype_category: Musculoskeletal_System_and_Connective_Tissue:other
phenotype:
  Previously diagnosed with Undifferentiated Connective Tissue Disease and Diffuse Connective Tissue Disease


human_id: hu3B032D
date: 2015-08-03 21:45:51
phenotype_category: Musculoskeletal_System_and_Connective_Tissue:other
phenotype:
  Multiple lumbar and cervical subluxaations, thoracic outlet syndrome, carpal tunnel syndrome, some hypermobile joints


human_id: hu7FC773
date: 2015-11-01 19:12:30
phenotype_category: Musculoskeletal_System_and_Connective_Tissue:other
phenotype:
  Hypermobility of the Joints, DDD, Osteopinia, Told I had Rheumatism  as a child. Bone Problems run in my family of a chronic pain.


human_id: huED93F6
date: 2015-11-20 12:42:57
phenotype_category: Musculoskeletal_System_and_Connective_Tissue:other
phenotype:
  osteopenia, cervical disc herniation x3, thoracic disc herniation x1, (sciatica is related to lumbar disc herniation x1)


human_id: hu7123C1
date: 2016-02-28 23:25:07
phenotype_category: Musculoskeletal_System_and_Connective_Tissue:other
phenotype:
  Medial meniscus tear left knee M23.204; Osteoarthritis knees bilateral M17.0; Wrist fracture left S62.002D


human_id: huE18D82
date: 2016-05-05 22:30:53
phenotype_category: Musculoskeletal_System_and_Connective_Tissue:other
phenotype:
  Ehlers Danlos Syndrome, Temporal Mandibular Joint Disfunction (TMJ), Bruxism, Recurrent Corneal Abrasion, Striae / Atrophic Scaring, Iliotibial Band Syndrome, Joint Hypermobility, Disassociated Trachea,


human_id: hu4EEA9B
date: 2016-07-29 19:34:44
phenotype_category: Musculoskeletal_System_and_Connective_Tissue:other
phenotype:
  None, but I have heard of several relatives suffering with various of the aforementioned surveyed conditions.


human_id: hu70ED6F
date: 2016-10-18 00:56:58
phenotype_category: Musculoskeletal_System_and_Connective_Tissue:other
phenotype:
  arthritis in left foot and right knee from previous injuries; foot injury approx. 20 years ago, knee injury approx. 10 years ago


human_id: hu0B51B8
date: 2017-06-22 01:12:10
phenotype_category: Musculoskeletal_System_and_Connective_Tissue:other
phenotype:
  I always feel like I have Rheumatoid arthritis and Fibromyalgia but they never diagnose me with those


human_id: huA5B645
date: 2012-10-19 13:15:18
phenotype_category: Nervous_System:other
phenotype:
  Aura without migrane. The symptoms are the same as the aura in "Migrane with aura" but I never get the migrane.


human_id: huB10361
date: 2013-01-09 13:34:02
phenotype_category: Nervous_System:other
phenotype:
  possible CIDP or other demyelinating disease, (CSF protein 380), history of positive Beta 2 Transferrin,   multiple nerve root diverticula throughout spine, cervical issues (osteophyte/endplate sclerosis, reversal of cervical lordosis, neuropathy, ataxia, parasthesias, double vision, tinnitus, hearing loss, neurogenic bladder, pain in spine


human_id: huA55602
date: 2013-03-13 17:20:46
phenotype_category: Nervous_System:other
phenotype:
  A total of four migraines with aura in my life after a car accident, then a total of three auras without headache.


human_id: hu2BA3AC
date: 2013-07-21 00:07:56
phenotype_category: Nervous_System:other
phenotype:
  hypnic jerk, sound/head motion-induced aura-like visual field disturbance (without epilepsy or associated migraine)


human_id: huC62047
date: 2013-12-23 21:12:41
phenotype_category: Nervous_System:other
phenotype:
  When I was young I used to have Recurrent sleep paralysis but was not diagnosed with this and have not had it in years


human_id: huCCF18D
date: 2014-03-02 11:38:28
phenotype_category: Nervous_System:other
phenotype:
  I carry a rare genetic mutation on the prion protein gene (PRNP) that is associated with familial prion disease.


human_id: huED0F40
date: 2014-03-02 13:41:34
phenotype_category: Nervous_System:other
phenotype:
  parathesia (pins & needles) of left forearm and hand, suspect as part of neurogenic thoracic outlet syndrome or cervical instability


human_id: hu816A0B
date: 2014-04-06 08:32:53
phenotype_category: Nervous_System:other
phenotype:
  Based upon my responses to an online screening quiz, I am most likely suffering from an obsessive-compulsive disorder.


human_id: hu5A625E
date: 2014-09-11 18:13:21
phenotype_category: Nervous_System:other
phenotype:
  Chronic Depression (medication non-effective), Chronic Pain Syndrome, Chronic Fatigue Syndrome, Asperger's Syndrome


human_id: huE34B72
date: 2014-12-11 12:35:00
phenotype_category: Nervous_System:other
phenotype:
  I have experienced periodic episodes of sleep paralysis. I have not been officially diagnosed with Narcolepsy, but multiple doctors has suspected it. My father has been diagnosed with Narcolepsy.


human_id: hu826751
date: 2014-12-19 20:36:55
phenotype_category: Nervous_System:other
phenotype:
  sleep-paralysis was non-diagnosed but happened a few times when I was younger.  I suspected caffeine intake might have been an instigating factorex


human_id: hu79C24D
date: 2015-11-11 05:26:46
phenotype_category: Nervous_System:other
phenotype:
  Insomnia, Unsure of specific ICD code. I also have frequent episodes of sleep paralysis but no formal diagnosis (and they may be subclinical).


human_id: huB17F67
date: 2017-07-04 14:40:33
phenotype_category: Nervous_System:other
phenotype:
  Hypersomnia, Somniloquy, Nightterrors and nightmares,  Ocular ache (not migraine), Attention deficit disorder, Anxiety disorder, Depression, Dyslexia, Asperger's


human_id: hu715C3F
date: 2017-07-10 18:34:14
phenotype_category: Nervous_System:other
phenotype:
  diabetic autonomic neuropathy, neurocardiogenic syncope, post-traumatic headaches and seizures, chronic pain syndrome, mild cognitive impairment


human_id: hu691345
date: 2017-11-29 15:48:40
phenotype_category: Nervous_System:other
phenotype:
  possible MS developing in low back area where disc herniation and arthritis caused myelin sheath damage to the spinal nerve root at L5-S1


human_id: huED0F40
date: 2013-01-09 23:35:13
phenotype_category: Respiratory_System:other
phenotype:
  Since 2005 an asthma-like reaction to spring tree pollen, requiring steroid inhaler for month of March to 1st or 2nd week of April, then remits


human_id: hu02A209
date: 2013-06-27 19:55:16
phenotype_category: Respiratory_System:other
phenotype:
  Breathing problems have resolved after daily ingestion of raw garlic cloves (3). Dragon breath but no coughing!


human_id: hu9745B5
date: 2014-03-27 00:12:09
phenotype_category: Respiratory_System:other
phenotype:
  father dx with nasal polyp resulting in annureysm, complicated by blood thinner medications for IhSS


human_id: hu53821E
date: 2014-09-29 15:55:48
phenotype_category: Respiratory_System:other
phenotype:
  Coccidiodomycosis - Fungal Infection requiring removal of lower lobe in right lung due to repeated bouts of pneumonia


human_id: hu4EEA9B
date: 2016-07-29 19:31:05
phenotype_category: Respiratory_System:other
phenotype:
  Mostly just allergies (I live in CA Central Valley), but have never needed an inhaler or anything else.  I have great lungs.


human_id: hu60AB7C
date: 2013-01-12 21:26:21
phenotype_category: Skin_and_Subcutaneous_Tissue:other
phenotype:
  My dandruff/itchy scalp stopped after adding anhydrous Betaine 750mg sublingual upon awakening every day minimum.


human_id: huF080F9
date: 2014-06-13 15:57:09
phenotype_category: Skin_and_Subcutaneous_Tissue:other
phenotype:
  For my answers above, if by "diagnosed", you mean "have had" --- don't really know of anyone going to a doctor to be "diagnosed" with dandruff!


human_id: hu369F3B
date: 2014-08-30 20:52:39
phenotype_category: Skin_and_Subcutaneous_Tissue:other
phenotype:
  I have dandruff but haven't been diagnosed by a physician. I have had some hair loss over the years but am not bald


human_id: hu4EEA9B
date: 2016-07-29 19:33:57
phenotype_category: Skin_and_Subcutaneous_Tissue:other
phenotype:
  I'm 30 and I still get blackheads and back acne.  Most likely from sweating, exercise, and high testosterone.  I am very fair-skinned.


human_id: huDD5D00
date: 2016-09-05 12:01:30
phenotype_category: Skin_and_Subcutaneous_Tissue:other
phenotype:
  At 34, I have the WORST acne in my life. During puberty it stayed confined to my face alone but not it's all over my ears, neck, shoulders, back and chest as well.


human_id: hu691345
date: 2017-11-29 15:55:44
phenotype_category: Skin_and_Subcutaneous_Tissue:other
phenotype:
  chronic problem with hair follicles getting plugged with sebum/keratin? Decreasing as I age. But my son also has this, as does my mother. Also, I my sister and I have both been told by dermatologists that we tend to "overcalcify" or deposit excess calcium in areas of infection or inflammation. Somewhat higher than average sensitivities to laundry soap or bath soap, causing itching, without rash.


human_id: hu4B2CE0
date: 2017-12-07 07:08:32
phenotype_category: Skin_and_Subcutaneous_Tissue:other
phenotype:
  Above-normal sebaceous production, extremely fragile nail cuticles and brittle fingernails with a tendency to peel


human_id: hu26B551
date: 2012-10-12 00:03:24
phenotype_category: Vision_and_hearing:other
phenotype:
  I began losing hearing in my late teens and most of my family members had hearing loss by middle age, with moderate to severe hearing loss in old age.


human_id: huA5B645
date: 2012-10-19 13:12:23
phenotype_category: Vision_and_hearing:other
phenotype:
  I experience aural headaches (scintillations lasting about 20-30 minutes without any pain - these are sometimes precursors to migrane headaches in other people, but I have never had a migrane.)


human_id: hu868880
date: 2012-11-11 22:04:05
phenotype_category: Vision_and_hearing:other
phenotype:
  Have also been diagnosed with vestibular disorder similar to Meniere but with perfect hearing (also no hearing loss with tinnitus)


human_id: huD09050
date: 2012-12-13 15:44:54
phenotype_category: Vision_and_hearing:other
phenotype:
  Early cataract (not age-related, not traumatic, probably genetic), torn retina, severe motion sickness susceptibility, labyrinthitis


human_id: huA099E6
date: 2013-03-04 10:13:38
phenotype_category: Vision_and_hearing:other
phenotype:
  strong myopia (-5.6 diopters, corrected by radial keratotomy some 30 years ago, high frequency hearing loss with low frequency hearing loss in left ear due to explosions near left ear (gun in a tank)


human_id: hu6D1115
date: 2013-04-28 22:57:41
phenotype_category: Vision_and_hearing:other
phenotype:
  I wear glasses for driving and reading, but I'm not sure what the diagnosis is. The condition is age related; I didn't wear glasses when I was young.


human_id: hu35020C
date: 2013-11-15 22:40:48
phenotype_category: Vision_and_hearing:other
phenotype:
  strabismus in both eyes, corrected when 5.  cataracts removed last year.  always worn corrective lenses


human_id: hu3DB8ED
date: 2014-08-29 22:50:16
phenotype_category: Vision_and_hearing:other
phenotype:
  I doctor said I had macular degeneration but it's not age related.   I was 24 years old at the time.


human_id: huD586B2
date: 2016-05-27 11:40:15
phenotype_category: Vision_and_hearing:other
phenotype:
  Difficulty clearing ears, tiny ear canals. As a child, some hearing issues on annual tests (though I never thought i had a problem) and saw many doctors who wanted to put "tubes" in my ears. Parents never allowed it.


human_id: hu7F50FF
date: 2017-03-13 15:42:59
phenotype_category: Vision_and_hearing:other
phenotype:
  have to wear prism glasses to drive because my eyes won't focus at distance; not sure what this is called


human_id: hu04D550
date: 2017-05-31 12:20:54
phenotype_category: Vision_and_hearing:other
phenotype:
  sude hearing loss right ear at age 32, never resolved. Concurrent loss of balance, resolved after several days. Concurrent tinnitus, never resolved.


human_id: hu008567
date: 2015-08-12 18:14:48
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I draw and paint almost equally with right and left hands. Fine motor skills virtually equal both hands.


human_id: hu008567
date: 2015-08-12 18:14:48
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  Born with red hair per adoption papers/description. Very thin until age 2 then VERY thick and wavy. Tiny streaks of gray all my life


human_id: hu98FFC6
date: 2015-08-13 02:27:07
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My mother had brown eyes (21).\n\nMy father had and sister has gray-green eyes (5). They seemed to change based on what they were wearing.\n\nBoth brothers have brown eyes like my mother's (21).\n\nMy husband and kids have eyes like mine (14).


human_id: hu98FFC6
date: 2015-08-13 02:27:07
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I was a strawberry blonde when very young and my hair became more prominently brown as I aged. I have very fine


human_id: hu98FFC6
date: 2015-08-13 02:27:07
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  hair that when gathered makes a skinny pony tail. It is not stringy-thin; it has body and very slight curl to it. I could never grow it longer than just below my shoulders. I also have a widow's peak and a slight cowlick left of center.


human_id: hu0FB755
date: 2015-08-15 02:37:33
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  Both parents were near sighted. I am near sighted in my right eye because of being in a incubator for 11weeks. This in January to March 1960


human_id: hu2D6140
date: 2015-08-18 15:32:08
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  born very blond and my hair color darkened over the years to a light brown.  At age 73 it I beginning to grey


human_id: hu4BF398
date: 2015-08-18 15:39:08
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I can't tell my eye color based on this.  I would have to look in mirror while holding color chart next to my eye.


human_id: huA60DA9
date: 2015-08-20 12:27:13
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I was born with a full head of dark brown hair. Had light brown hair through most of my childhood. Hair started darkening around puberty to the medium brown shade it is now.\n\nMy brother who was born with blue eyes that later turned brown was also born with straight blonde hair that turned brown and extremely curly when he hit puberty (it has since stayed brown and extremely curly).


human_id: hu5A063B
date: 2015-08-21 08:55:24
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  my left eye pupil is slightly larger. my dad has light blue eyes and my mom has green eyes. my sister's eyes are blue on the outer iris and orange around the pupil. my pupils are always huge for no reason unless im looking directly into light. i can move my right eye independent of my left eye


human_id: hu5A063B
date: 2015-08-21 08:55:24
phenotype_category: Basic_Phenotypes:Hair Color - Text Description
phenotype:
  ash blonde (the color of wet sidewalk... that color that is neither blonde nor brown...aka grey but not from age)


human_id: huB10361
date: 2015-08-21 16:54:18
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  yes- my eyes have a rusty color surrounding the iris that was not there before- I also have had lesions for two years


human_id: hu2C1AB7
date: 2015-08-25 00:24:54
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My parents have always informed me my eyes have a history of "changing color" depending on my mood and the lighting. Often golden "flecks" and a golden hue is what my mom would use to describe my eyes


human_id: hu2C1AB7
date: 2015-08-25 00:24:54
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I was born with very very blonde hair. Almost platinum blonde. It wasn't until the age of 5 or 6 that my hair started to darken up and become more of a dirty blonde. By then


human_id: hu8D99F6
date: 2015-08-25 13:48:04
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  Father's eyes: Ice-blue iris with some lighter and darker blue variations (most like image #4)\nMother's eyes: Solid medium dark brown (most like #20 but with fewer variations)\n\nIf asked


human_id: hu8D99F6
date: 2015-08-25 13:48:04
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  everyone will say I have brown to dark brown eyes and are surprised when they get a close look to see much of my outer iris is green.


human_id: hu8D99F6
date: 2015-08-25 13:48:04
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I had dark blond (golden hair) that steadily darkened until it was dark brown but my mid-teens.\n\nMy father was similar though he progressed to nearly black hair.\n\nMy mother had a consistent medium-to-dark brown hair with red highlights her entire life.


human_id: hu95E46D
date: 2015-08-25 15:54:03
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  can't get weight off! Never was this heavy previously. Getting gastric sleeve in December. If any of this is relevant... :)


human_id: hu95E46D
date: 2015-08-25 15:54:03
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My mother and younger brother have dark brown eyes; my father and older brother grey. My maternal grandmother had unusual yellowish amber brown  "wolf eyes". (She was 1/2 Danish%2C 12.5% Scottish and 37.5% West Indian African). Both of my grandfathers had brown eyes


human_id: hu95E46D
date: 2015-08-25 15:54:03
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  (out of 4 siblings-all others brown) and as does one maternal aunt (out of 3%2C other 2 with dark brown eyes). All of my father's 4 siblings have grey-blue eyes.


human_id: hu95E46D
date: 2015-08-25 15:54:03
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I was born BALD!! And did not seem to grow any amount of hair on my head until at least 2 years old. Then


human_id: hu95E46D
date: 2015-08-25 15:54:03
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  and stayed that way until I cropped it all off in a boy's pixie skullcap style at the age of 7. It grew back in much


human_id: huDBF9DD
date: 2015-08-26 10:31:02
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I remember having a contest with a girl in high school where we would compare whose eyes were darker brown (this was during biology class


human_id: huDBF9DD
date: 2015-08-26 10:31:02
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  of course%2C when we should have been paying attention).  My eyes look less brown than I remember.  It's as if I have the suggestion of a lighter brown more towards the outside now


human_id: huDBF9DD
date: 2015-08-26 10:31:02
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  hinting towards green but not there yet.  I would say this is more in the left eye than the right.   I did have Lasik for nearsightedness  in 2003


human_id: hu034DB1
date: 2015-08-26 11:00:27
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My eye color has changed from blue to green since birth. My eyes are now similar to the eye color of my father


human_id: hu627574
date: 2015-08-26 12:45:23
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  then in my 20's turned a bit darker.  I started getting some gray hair around 26 and I am almost all gray at 55.


human_id: hu7123C1
date: 2015-08-26 21:07:41
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My weight has varied over the years from 165 to 225 lbs. I am trying to work on getting regular exercise and cutting back on caloric intake. Have lost 30 lbs over the past 5 years. My goal is another 30 lbs in 5 years. I am an "End to end section hiker of the Appalachian Trail


human_id: hu7123C1
date: 2015-08-26 21:07:41
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  with goal to reach the half-way mark at 1100 miles in PA on my 70th birthday in 2016 and complete all 2200 miles atop Katahdin ME on my 75th birthday September 10


human_id: hu7123C1
date: 2015-08-26 21:07:41
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  but must have had a parent (I did not know my mathernal grandparents) with blue eyes. 3 of my 7 siblings have blue eyes with blond hair (as a child) like me


human_id: hu7123C1
date: 2015-08-26 21:07:41
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  and gradually darkening to brown as an adult from age 21 to 50 yo; and with aging from 51 to 69 yo increasing gray (initially in beard and then scalp).


human_id: hu7123C1
date: 2015-08-26 21:07:41
phenotype_category: Basic_Phenotypes:Any final thoughts?
phenotype:
  brown eyes. Two of my children have hazel eyes and dark hair; One daughter blue eyes and blonde hair.


human_id: huE9B080
date: 2015-08-26 23:42:50
phenotype_category: Basic_Phenotypes:Any final thoughts?
phenotype:
  I liked the eye pictures for reference.  You should do hair color too. Also should have body silhouettes to pick closest match.


human_id: huC14AE1
date: 2015-08-27 10:55:27
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My eye color has remained the same since birth.  They are both a uniform blue color without significant patterning.


human_id: huCBEE5B
date: 2015-08-27 14:39:47
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  Eye size is slightly asymmetric. Had above average visual acuity for most of my life in both eyes. Last eye exam placed me at 20/20.


human_id: hu9408BD
date: 2015-08-27 17:22:12
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I am ambidexterous in the sense that there are things I do best with my left hand and others I do best with my right hand.


human_id: hu52DA79
date: 2015-08-28 15:45:01
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  and began to darken towards brown when I was about 30. They've gotten progressively darker each year. My father had clear medium green eyes


human_id: hu63432C
date: 2015-08-29 11:22:52
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  Born with black hair which fell out when I was about one. Hair grew back blonde and began to darken when I was approximately 7 or 8.


human_id: hu3E50D4
date: 2015-08-29 11:25:37
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I just gained 15 pounds while on prednisone.  My normal weight is between 135 and 140.  I am now off prednisone and hoping to lose the extra weight.


human_id: hu3E50D4
date: 2015-08-29 11:25:37
phenotype_category: Basic_Phenotypes:Any final thoughts?
phenotype:
  My very wavy/curly hair has gone straight except for one big wave in the front.  My father had hair like mine used to be and my mother had hair like mine became after age 72.  I know my father was heterozygous for curl/straight and my mother homozygous for straight.  My sisters both have straight hair.


human_id: hu265361
date: 2015-08-29 11:30:25
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My hair became much darker during and after my 3 pregnancies but eventually returned to a medium brown.


human_id: huCCF26A
date: 2015-08-29 11:34:59
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My siblings (7) total have eye color ranging from hazel to the blue color I have. My eye color is frequently remarked upon by strangers and friends.


human_id: huCCF26A
date: 2015-08-29 11:34:59
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I was tow-headed until puberty but my hair remained light brown until it started turning gray in my late 40s. I have family members who turned gray very early


human_id: huCCF26A
date: 2015-08-29 11:34:59
phenotype_category: Basic_Phenotypes:Any final thoughts?
phenotype:
  I also have a family history of macular degeneration and have wondered if eye color and that eye condition are related.


human_id: hu4F3A99
date: 2015-08-29 11:36:11
phenotype_category: Basic_Phenotypes:Any final thoughts?
phenotype:
  I needed no glasses until about 58.  Now at 67 my eyes are very bothersome.  My distance vision needs only slight correction but close in my eyes point in different directions left/right and up/down AND they have different corrections


human_id: huF041C5
date: 2015-08-29 11:44:17
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  my father & his father all = same medium/darkish brown eyes.\n- My father's mother = blue eyes.\n- My sister & mother = green/blue-ish eyes. (Not sure about mother's parents)\n\n- Myself


human_id: huF041C5
date: 2015-08-29 11:44:17
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  all from a young age. My father's father wore trifocals but don't remember details of his eyesight.\n- My sister & mother = perfect vision except for very very mild age-associated need for reading glasses in her mid/late 40s for my mother.


human_id: huF041C5
date: 2015-08-29 11:44:17
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  thin. Does get reddishauburn with a lot of sun exposure (which is why people seem to think it's my "natural" color when I use henna to make it redder).


human_id: hu14262A
date: 2015-08-29 11:44:44
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My eyes have always been blue.  The eye colors in your chart look more gray than blue - but perhaps my computer just does not show them correctly.  \n\nFamily: My dad was Jewish and had brown eyes. My mother is not Jewish and has greenish eyes. One of my sisters has brown eyes and one has greenish-blue eyes.


human_id: hu14262A
date: 2015-08-29 11:44:44
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I was very blond as a small child. Dark blond in teens and early 20s. Hair turned brown in my 30s and just kept getting darker and darker but I also started getting a few gray hairs when in late 30s early 40s. I am now 64 and still have mostly brown hair but maybe 35-40% is turning gray according to my hairdresser. My hair is much less gray than anyone else my age that I know


human_id: hu14262A
date: 2015-08-29 11:44:44
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  for some reason. There is lots of gray in back near my neck and some gray near my ears. The rest of my hair just has gray hairs distributed throughout the brown. Not that you care


human_id: huCAFC1C
date: 2015-08-29 11:54:20
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  There is a history of glaucoma on my mother's side.  There is also a history of dark brown eyes with blue rings around them


human_id: hu6C3F34
date: 2015-08-29 11:56:47
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  Somewhat ambidextrous. I play all sports right-handed; can play racquetball with myself (right hand vs. left hand)


human_id: hu6C3F34
date: 2015-08-29 11:56:47
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  there is more green around the edges of the iris than when I was younger. My maternal grandfather had green eyes


human_id: hu76CAA5
date: 2015-08-29 12:10:57
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  my daughter's risk of macular degeneration is 5 times greater than average. My eyes are considerably smaller than average


human_id: hu76CAA5
date: 2015-08-29 12:10:57
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  darkening as I aged until appearance of first gray in circa age 40. Very grey now at age 62 (my hair is almost as grey as my 90 year old mother). Oddly


human_id: hu76CAA5
date: 2015-08-29 12:10:57
phenotype_category: Basic_Phenotypes:Any final thoughts?
phenotype:
  My overall physical traits phenotype is much closer to my father than my mother. Currently trying to sort out HLA inheritance. Received assistance with HLA*IMP software which imputed these haplotypes from my whole genome VCF file (with probabilities) -\n\nallele1 allele2 probability\n\nHLA-A* 03:01 26:01   100%  55%\n\nHLA-B* 38:01 40:01   96%  86%\n\nHLA-C* 12:03 07:02   100%  99%\n\nHLA-DRB1* 04:04 09:01   82%  100%\n\nHLA-DQA* 03:01 02:01    99%  76%\n\nHLA-DQB1* 03:02 03:03   99%  98%\n\nHLA-DPB* 04:04 09:01   82%  100%\n\nThe HLA*IMP software was done for me


human_id: hu76CAA5
date: 2015-08-29 12:10:57
phenotype_category: Basic_Phenotypes:Any final thoughts?
phenotype:
  so I am quite anxious to know how reliable these haplotypes might be. Potential implications for autoimmune disorders in my family (just started treatment for psoriatic arthritis after 5+ years of odd signs & symptoms - diagnosis based on lab work and X-rays). This and cytochrome P450 imputations are perhaps the most important info that a participant can derive from whole genome results. Can we consider blanket application to all participants??\n\n\n\n


human_id: hu10D50B
date: 2015-08-29 12:17:57
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  This seems to be incredibly dependent on the source of lighting. I felt I could replicate the conditions depicted in the example photographs by shining my phone's camera flash/flashlight 6 inches from my eye.


human_id: huD20DAF
date: 2015-08-29 12:55:54
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I have always had two different eye colors.  No one else in the family seems to have this anomaly.  Some of us have dry eyes


human_id: huD20DAF
date: 2015-08-29 12:55:54
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  but we do live in the west where it is very dry.\nThe right eye lid started drooping when I was about 40.  I had a brow lift to fix this problem


human_id: huD20DAF
date: 2015-08-29 12:55:54
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  but the drooping began again at about age 60.  \n\nFloaters in the eye began about age 50.  They are very distracting.


human_id: huD20DAF
date: 2015-08-29 12:55:54
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I still would describe my hair (question3.1) as dull red with gray and white saturation.  It is hard to answer question 3.1 with the answers provided.  Original pre-aging hair color was light red or copper-ish.


human_id: huF80F84
date: 2015-08-29 13:08:12
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  when I wear an olive green shirt my eyes are almost a perfect match. The lineup is especially hard for me because I've seen my eyes look like 7


human_id: huF80F84
date: 2015-08-29 13:08:12
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  but they look like 11 most today (I used a bright LED in front of my mirror to check). I have the golden-brown ring in the center. It's probably between the ring in 9 and 11.


human_id: huF80F84
date: 2015-08-29 13:08:12
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  When exposed to the sun I get very very blonde highlights to the point where in pictures of me from summers where I played sports or was outside a lot in general


human_id: huF80F84
date: 2015-08-29 13:08:12
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  and it lightened up. If you look at my hair very closely there is a wide range of browns from strawberry blonde to blonde to dark brown -- When I dyed my hair blue without bleaching it first I got blue


human_id: huA55602
date: 2015-08-29 13:16:25
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I was ambidextrous when young and my kindergarden teacher had me use my right hand.  One of my children is very ambidextrous (writes left%2C golfs and eats right) and the other child completely left handed.


human_id: huA55602
date: 2015-08-29 13:16:25
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  they became greenish at about 18 and have gotten more green as I age.  They are in between photos 13 and 14.


human_id: hu9941AD
date: 2015-08-29 13:17:32
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My eyes have lightened only slightly since early childhood.  Some of my four children's eyes (all blue or blue with hazel rings or flecks) have lightened through the years (oldest is only 12%2C youngest not yet four).  My younger sister's blue eyes lightened a lot more than mine


human_id: hu9941AD
date: 2015-08-29 13:17:32
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  and I've noticed the two of my children with hazel elements in their blue eyes have had their blue lighten up more than the other two.  My nearly-four-year-old daughter has dark blue eyes and looks almost identical to what I did at that age (not just eyes%2C but overall).  I doubt hers will lighten much; they haven't yet.\n\nMy paternal side of family are all blue-eyed


human_id: hu9941AD
date: 2015-08-29 13:17:32
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I've observed through the years that the dark-haired (med to dark brown) ones of us have kept a darker spectrum of blue in our eyes


human_id: hu9941AD
date: 2015-08-29 13:17:32
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  while the lighter-haired (light brown to blonde) members tend to be the ones whose eyes have lightened more.\n\nI have high-degree myopia (-9.50 and -10.00 glasses prescription; -8.00 and -8.50 in contacts).  Some members of my family also have myopia but not nearly as bad as mine.  My sister is the closest


human_id: hu9941AD
date: 2015-08-29 13:17:32
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  and her contacts prescription is around -3.25. \n\nI almost forgot. My maternal side of family all have lighter blue eyes or greenish-blue.


human_id: hu9941AD
date: 2015-08-29 13:17:32
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  but then darkening again to a dark medium brown. Three of my four children have followed the same pattern: dark brown when born


human_id: hu9941AD
date: 2015-08-29 13:17:32
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  then darkening again.  Last child has maintained dark-medium brown hair since birth to current age of nearly four.


human_id: hu9941AD
date: 2015-08-29 13:17:32
phenotype_category: Basic_Phenotypes:Any final thoughts?
phenotype:
  Irish descent.  White American maternal grandfather (don't know history).  Both my paternal grandparents were half Scottish


human_id: hu9941AD
date: 2015-08-29 13:17:32
phenotype_category: Basic_Phenotypes:Any final thoughts?
phenotype:
  half German. I attribute my dad's side of the family's members all sporting piercing blue eyes to the German descent.


human_id: huD0E08A
date: 2015-08-29 13:23:07
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  Most have light blue/grey eyes on my dad's side with a few being brown and a couple blue/green. My mother's side tend to be brown with a few green/grey


human_id: hu28DA07
date: 2015-08-29 13:31:27
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  but I said 6'2" because that's  what I have been for most of my life until age took a couple of inches from me.


human_id: hu6D50BE
date: 2015-08-29 13:56:59
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  and my father referred to his as "hazel" though I never knew what that really meant...and don't remember exactly what color description I would have used for them.  Maybe just "brown" as I always thought of mine


human_id: hu599905
date: 2015-08-29 13:58:05
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  my sideburns and bear were distinctly red. Everything is gray enough now that no red tones are noted at all.


human_id: hu5AB9A8
date: 2015-08-29 14:45:54
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My grandfather had the most remarkable gaslight blue eyes. Mine are much more common blue by comparison.


human_id: hu6D1115
date: 2015-08-29 15:16:29
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  Her mother's eyes were true blue. My father and his parents had brown eyes. I recall my maternal grandmother's eyes being more of a light brown


human_id: hu6D1115
date: 2015-08-29 15:16:29
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  very pretty.\n\nMy eyes are more grayish brown at the outer part and darker brown as they get closer to the pupil.


human_id: hu6D1115
date: 2015-08-29 15:16:29
phenotype_category: Basic_Phenotypes:Hair Color - Text Description
phenotype:
  but it sunbleached to blond highlights easily and I also had red highlights so that if I stood in sunlight people would say Oh you've got red hair!


human_id: hu6D1115
date: 2015-08-29 15:16:29
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  but I have pictures of me at the age of 6 or 7 where it appears to be blonde.The sun definitely lightens my hair. I always loved my hair color and texture


human_id: hu6D1115
date: 2015-08-29 15:16:29
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  there is red in my hair. My sister was a strawberry blonde as a child. My father's beard would grow out red. My mother was blonde as a child; later her hair was light brown.


human_id: hu96405F
date: 2015-08-29 15:31:45
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  but am left-handed for anything that requires a two-handed grip (holding a baseball bat or a broom%2C for instance).


human_id: huE9D7FD
date: 2015-08-29 15:42:52
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My hair color is dark brown a reddish tone. When I was born it was black. It then grew in a lighter shade of brown. It darkened when I was a teenager to the color it is today.


human_id: hu34BA70
date: 2015-08-29 15:50:37
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  just green.  They've always been the same color.  No one else in my family has green eyes.  Both parents had blue eyes


human_id: hu34BA70
date: 2015-08-29 15:50:37
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  no one else in my family has my blood type.  All my brothers and sisters /have/had type O.  Both parents had O.  I


human_id: hu00D419
date: 2015-08-29 15:56:36
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My hair color at 60 years of age still matches the color of samples of my  hair saved from when I was a small child except that there is now a great deal of gray hair in places.


human_id: hu30888B
date: 2015-08-29 16:39:27
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  and hair on other parts of my body is also red.  The red hair went gray first so there is only hints of red here and there now.


human_id: hu70C80B
date: 2015-08-29 18:20:49
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I don't know birth color - to my recollection the "brown" that my eyes are has always been about the same.


human_id: huD554DB
date: 2015-08-29 20:06:03
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  Left eye has scaring similar to macular degeneration but eye doctor thinks is maybe mitochondrial related


human_id: huF8AE42
date: 2015-08-29 20:22:46
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  The golden band in my left eye matches the angular position of a congenital depigmented spot in my retina.  As far as I know this is not hereditary.\n\nMy family considers the dark rings around the outer edge of the iris to be a family trait (mother's side).


human_id: huF8AE42
date: 2015-08-29 20:22:46
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  which darkened as we hit elementary school age.  I found a single white hair when I was 25 and have been acquiring more very slowly since then.  They are scattered


human_id: hu5E55F5
date: 2015-08-29 20:24:55
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My eye color is quite different from at birth (was a light blue). I have had several eye infections and the drugs have changed the color of my iris in both eyes. Also I have scar tissue on both eyes


human_id: huA8B443
date: 2015-08-29 20:31:03
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  every thing else I do is left handed. i consider myself left handed. i was not forced to write righty as a child. \nI throw and eat lefty


human_id: huD95DAB
date: 2015-08-29 20:52:07
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I've always lightened/colored my hair and have always had trouble with my hair turning out with too much gold/red.


human_id: hu26B551
date: 2015-08-29 21:25:11
phenotype_category: Basic_Phenotypes:Left Eye Color - Text Description
phenotype:
  with only a touch of greenish brown near the pupil. A dark blue ring around the outer edge of the iris.


human_id: hu26B551
date: 2015-08-29 21:25:11
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  like our father. We are quite fair-skineed and prone to cataracts. My ophthalmologist says I have a blonde fundus.


human_id: hu57C3BB
date: 2015-08-29 21:38:52
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I was initially brown with curly hair which stayed that way until I was about 2 years old. Then it became straight.


human_id: hu5F5EB7
date: 2015-08-29 22:56:07
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My eyes don't really match any of the pictures they are very green with an almost black ring.  I don't know if they have changed color from the color at birth.  They have been green for as long as I remember.  My five siblings have either blue/grey or green eyes.  My mother my sister and I are long sighted and I have astigmatism.


human_id: hu05AE3F
date: 2015-08-29 23:09:41
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  You might want to consider a picture system similar to the eye color section with different hair types.  There are a few typing systems that some stylists use that you could model it off of (such as http://www.naturallycurly.com/hair-types


human_id: huE44F41
date: 2015-08-29 23:24:32
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  Had white blonde hair from babyhood through  childhood. Was a dirty dish water blonde by Jr. Highschool.


human_id: hu9745B5
date: 2015-08-30 01:12:24
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  Father is African American with dark brown eyes (skin tone like Bill Cosby); mother is Caucasian (German/Welsh- skin tone pinkish/ruddy pale) with light cornflower blue eyes. My only sibling (older brother) looks more biracial (darker skin tone with afro and brown eyes) but strong large build favoring my mother's side. My skin and hair are primarily light beige gold


human_id: hu9745B5
date: 2015-08-30 01:12:24
phenotype_category: Basic_Phenotypes:Hair Color - Text Description
phenotype:
  naturally beige blone with ash tones- recently greying around temples in a shocking white shade from temples to crown and a few single strands beyond that.


human_id: hu9745B5
date: 2015-08-30 01:12:24
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  progressing to more beige in my 30's and now os beige with golden blonde accents. I'm told the undertone is ash


human_id: hu9745B5
date: 2015-08-30 01:12:24
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  but never dark enough to be brown. The "grey" hair coming in from temple to temple started at age 42 and is more a bright and white


human_id: hu9745B5
date: 2015-08-30 01:12:24
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  only going back 1/4 inches into my crown area. Very annoying. Hair on legs and arms has always been fine light gold blonde.


human_id: hu9745B5
date: 2015-08-30 01:12:24
phenotype_category: Basic_Phenotypes:Any final thoughts?
phenotype:
  but there were some blondes on her side. So I basically picked up only the recessive genes in my parents and have no idea why so many showed up in me


human_id: hu9745B5
date: 2015-08-30 01:12:24
phenotype_category: Basic_Phenotypes:Any final thoughts?
phenotype:
  whereas my older brother is a more obvious blend of our parents. There is no error in the DNA - this is my actual blood family- but I look like an odd duck because of my small size


human_id: hu2D6140
date: 2015-08-30 01:20:50
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I had very light blond hair as a child and it darked as I matured to a light brown.  At age 73 I have visible gray at the temple and in other areas.  My father also grayed late


human_id: hu117D1E
date: 2015-08-30 07:08:27
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My family has mainly light blue or grey eyes. I have the dark eyes of hazel or green eyes. My eye color may change from blue to grey to green


human_id: hu86BC6B
date: 2015-08-30 07:20:38
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  Had blue eyes until around age 7 or so. My eyes have always been very sensitive to light. I also have photic sneeze reflex


human_id: hu86BC6B
date: 2015-08-30 07:20:38
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  my eye color seems to shift from a lighter green to a more intense green depending on the circumstances.


human_id: hu86BC6B
date: 2015-08-30 07:20:38
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  Bon with very blonde hair. Hair has progressively gotten darker as I've aged. Hair still lightens significantly with sun exposure. Hair still on the very light end of the brown spectrum.


human_id: hu2C7459
date: 2015-08-30 10:41:47
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  changed to green in childhood (between 6 and 12). This change is common in my maternal family. Strong family history of myopia


human_id: hu90D19A
date: 2015-08-30 11:39:46
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  born with strawberry blonde hair turned to a darker blonde when I got older. During my first pregnancy my hair turned brown and never turned back.


human_id: hu2E4B9F
date: 2015-08-30 15:28:57
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  but they have a tint of green overall. All members of the family have brown eyes of varying shades all leaning to the dark rather than light brown. My mother developed macular degeneration in her late sixties. She died at 70 still seeing well enough to drive. All members wear corrective lenses and have since early teens with the exception of me. I started wearing glasses 45.


human_id: hu2E4B9F
date: 2015-08-30 15:28:57
phenotype_category: Basic_Phenotypes:Any final thoughts?
phenotype:
  Father had black hair turned grey. Mother had red hair turned grey. Two brothers have brown hair. One brother my sister and myself all redheads.


human_id: huFF2969
date: 2015-08-30 15:44:09
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  Blood type is my best guess from years long past.  My doctor no longer keeps it in my medical records.


human_id: hu9FEC32
date: 2015-08-30 17:08:26
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  It is possible I was "turned around" as a lefty when I was a child.  I remember being told to hold my pen in my right hand


human_id: hu6E8157
date: 2015-08-30 19:05:36
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My eyes are unchanged (insofar as I remember) since my youth (I'm 48 now).  My biological sister (same parents) had blue eyes as a child


human_id: hu6E8157
date: 2015-08-30 19:05:36
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I am beginning to gray around the temples.  \n\nWhen I was younger (18-35?) about 1/2 my facial hair was dark brown (like my scalp hair)


human_id: huD7960A
date: 2015-08-30 22:29:40
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  strong tendency to gain weight -- have been 245 lbs previously. Severe lifestyle changes bring me down to 165 lbs.


human_id: hu13812F
date: 2015-08-30 22:30:27
phenotype_category: Basic_Phenotypes:Any final thoughts?
phenotype:
  My daughter (2 years) also was born with very light blond hair. Seems to be getting darker (also blue eyes).


human_id: huC11596
date: 2015-08-30 22:38:46
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  if it were more green and less blue.  Then it slid back and stopped very close to #14.  \n\nMy mother's eyes went from hazel to true blue by the age of 50


human_id: huC11596
date: 2015-08-30 22:38:46
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  but I'd thought that eye color didn't change.  (My brother's eyes were always blue--both my parents are hazel.)


human_id: huC11596
date: 2015-08-30 22:38:46
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  turned red-blonde then straight blonde by the time I was 1 years old.  Then it gradually darkened with age.  By 18


human_id: huC11596
date: 2015-08-30 22:38:46
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  it's medium brown and still getting darker!  Zero gray.  Not a single hair.  But one grandmother was completely gray at 40


human_id: hu8A71D6
date: 2015-08-31 02:56:10
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I have a hx of chronic uveitis and am HLAB27+. I'm the only person in family on either side who has had this. Mother had extremely light blue eyes- approximately a # 1 on the chart. I have had "pigmented lenses" since at least age 30 per optomitrist. (Rentinal Pigmatosis?) Have needed glasses since age 8. Prescription is now -4.75 in both eyes. Glaucoma


human_id: hu8A71D6
date: 2015-08-31 02:56:10
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  even if cloudy out. Floaters since age 20. I would estimate 60-100 floaters in right eye and about half of that in left.


human_id: hu8A71D6
date: 2015-08-31 02:56:10
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I have extremely fine hair similar in width to that of a baby's.  The amount of hair on head is above average per hairdressers. It takes a long time to dry per hairdressers. I'm also hirsute and have had laser hair removal to full legs. I was born with red hair that quickly developed into blond that first year until i was about 3 y.o. Then it turned to light brown


human_id: hu8A71D6
date: 2015-08-31 02:56:10
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  then to dark brown with red highlights. Now just mousy brown. No gray. Stick straight. Hard to hold any style. Prominent part in scalp. Blue toned scalp. \n\nMy mother has red hair and everyone on her side is blonde or red with stick straight hair. Everyone's hair on my dad's side is black and wavy or curly.  I have wiry black and thick eyebrows like everyone on my dad's side.


human_id: hu8A71D6
date: 2015-08-31 02:56:10
phenotype_category: Basic_Phenotypes:Any final thoughts?
phenotype:
  I have a "cefe au lait" birthmark on my upper left thigh which all females on my dad's side have to varying degrees. I find it fascinating that there is actual code in our genetic material for such a specific birthmark placement on the skin!


human_id: hu3BBB0F
date: 2015-08-31 22:33:38
phenotype_category: Basic_Phenotypes:Right Eye Color - Text Description
phenotype:
  Hazel with brown stellate pattern darkest surrounding the iris and thinning towards the border of the iris. Coloring is evenly Bruce distributed brown to green


human_id: hu3BBB0F
date: 2015-08-31 22:33:38
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My maternal grandmother had glaucoma in her later years. My eyes were greener when I was younger.My father had Blue/grey eyes


human_id: hu3BBB0F
date: 2015-08-31 22:33:38
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  is 18 through 20's it was honey blonde and currently at age 55 it's  medium brown with natural light brown highlights and beginnings of some gray hairs around my face


human_id: hu620F18
date: 2015-08-31 22:46:23
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  Green eyes.  Hair has naturally changed over my lifespan.  It was curly red hair at birth (not orange%2C but a deep red).  It lightened to a honey blonde in childhood


human_id: hu620F18
date: 2015-08-31 22:46:23
phenotype_category: Basic_Phenotypes:Any final thoughts?
phenotype:
  Eye photos lacked any green eye examples.  Please consider having participants send a jpg of each eye.  Hair color variations are significant so consider photos to choose from or a combination of colors.


human_id: hu69F26B
date: 2015-09-01 09:37:08
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  Born with the same color hair. It shows blonde or reddish highlights when exposed to a lot of sun over time.


human_id: huC4A276
date: 2015-09-01 14:19:50
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I write and eat with my left hand but use scissors with my right and use both equally for things like mousing on a computer.


human_id: hu602487
date: 2015-09-02 03:02:54
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  Blue runs strongly in the family.\nOne granddaughters has such blue eyes that people comment on them.\nOne son has green eyes as does one of his daughters. \n


human_id: hu602487
date: 2015-09-02 03:02:54
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  As a baby and toddler I had very light blond hair -- it looks white in photos. \nIt darkened to dark blond by my 20's


human_id: hu839A25
date: 2015-09-02 23:16:47
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  changing gradually to green brown. Several family members on my mothers side of the family have had some degree of changing eye color after birth.


human_id: huB220C0
date: 2015-09-04 10:16:57
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  stayed that way until going gray about two years ago. Very light and wispy as a child. Thicker later. Remains curly.


human_id: hu005EB9
date: 2015-09-05 13:39:48
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  is pretty bad. The stress of its elongation may cause a retinal detachment. It is something that is monitored. I do think I have excellent color vision.


human_id: hu005EB9
date: 2015-09-05 13:39:48
phenotype_category: Basic_Phenotypes:Any final thoughts?
phenotype:
  Other little oddities: Big toes are not longest toes; index fingers are shorter than ring fingers; hard to do the Vulcan peace sign with left hand because fingers won't separate. Can barely manage it with right hand. Can roll tongue. Earlobes are not attached.


human_id: huB1488D
date: 2015-09-06 10:05:09
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I was born with blonde hair. It took on both a darker and more reddish hue at about age 13-14. My hair began turning gray at age 23.


human_id: huB1488D
date: 2015-09-06 10:05:09
phenotype_category: Basic_Phenotypes:Any final thoughts?
phenotype:
  It would have been nice to have a hair color reference photo set similar to the one used in the eye color section of the survey. I believe Manfred Kayser's group (Walsh et al.) had published one with their HIrisPlex. Also in future iterations you might consider exploring apps that allow smartphones to serve as reflectometers so you could get quantifiable data for the pigmentation analyses.


human_id: huED0F40
date: 2015-09-10 06:41:59
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  shown in pictures from childhood. Significant myopia began developing at 12. Choroid nevus diagnosed in mid-30's of brown spot on back of my right eye. Father had presbyopia when I was born


human_id: huED0F40
date: 2015-09-10 06:41:59
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  mother myopic with her self-described "coke-bottle glasses." Radial keratotomy at 24 improved both eyes' vision substantially but astigmatisms in both eyes and eye-strain headaches from uneven vision and computer time had me back in mild corrective lenses by age 28 when I had been glasses free for those 4 years


human_id: huED0F40
date: 2015-09-10 06:41:59
phenotype_category: Basic_Phenotypes:Any final thoughts?
phenotype:
  5'7"; my father's side of the family has most children over 6'3" with a very few 5'8" stocky males with more body hair. Your survey avoided morphic body builds: ectomorph


human_id: huED0F40
date: 2015-09-10 06:41:59
phenotype_category: Basic_Phenotypes:Any final thoughts?
phenotype:
  etc. Males with my surname tend to have long slender limbs and builds w/ low muscle mass. I have a thicker neck & broader shoulders than that norm


human_id: hu836D0A
date: 2015-09-10 15:32:46
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  usually one maternal family member in each generation has green\n\nall those who do have some lymphatic system issues including self (eye and ankles failure to drain properly causing swelling/cystic)


human_id: hu836D0A
date: 2015-09-10 15:32:46
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  seem to have hit all colors over the years\nborn bald til 3 yrs old\nwhite\nblond\nred\nstrawberry red\nbrownish red\ndarker brownish


human_id: hu3E2659
date: 2015-09-11 02:19:14
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My eyes at birth were a slightly lighter color blue gray and only darkened slightly as I aged based on looking back a photos.


human_id: hu3E2659
date: 2015-09-11 02:19:14
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My hair was a medium brown when I was born and now dark black in color. My hair is naturally straight and oily. I have two natural cowlicks one at the edge of my hairline on my forehead's right bang and the second at the back top of my head where the hair spirals.


human_id: hu91FB6B
date: 2015-09-13 11:35:49
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  \nthen increasingly dark blonde in childhood; \nlight brown by late adolescence or adulthood;\nnow lightening as it starts to go gray


human_id: hu151DB6
date: 2015-09-13 14:34:37
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  but it's not how I was taught so it's slower.  I have a  natural tendency to do many other things left handed


human_id: hu172277
date: 2015-09-14 11:29:14
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  unsure about eye color at birth\nmother has green eyes with orange/brown in center\nfather has blue eyes\nsibling has blue eyes


human_id: hu49F623
date: 2015-09-15 22:32:54
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I had rust reddish hair as a kid before it turned deep dark black hair. at least that is what i was told.


human_id: hu3B173B
date: 2015-09-16 10:09:12
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  as a toddler my hair was more red looking than brown.  As I got older it turned brown.  By the time I was 25 it was becoming gray.  By the time I was 35 it was probably all gray (not sure since I have colored it since age 25)


human_id: hu3B173B
date: 2015-09-16 10:09:12
phenotype_category: Basic_Phenotypes:Any final thoughts?
phenotype:
  my height seems to have decreased by a 1/2 inch. It is hard to tell given the measurement at a Dr office is not very precise.


human_id: hu3CEAE6
date: 2015-09-20 14:38:35
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My eyes are mostly a blue-grey color but there is a tiny bit of brownish green right at the edge of my outer iris.


human_id: hu3CEAE6
date: 2015-09-20 14:38:35
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I was born with jet-black hair that quickly lightened as I got older. It became very blonde by the time I was 3 or 4.


human_id: hu299FA0
date: 2015-09-22 16:25:23
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My irises sometimes look bluer and sometimes more hazel. It depends on the day (and probably mostly the background light)


human_id: huCBDC6D
date: 2015-09-22 19:26:33
phenotype_category: Basic_Phenotypes:Any final thoughts?
phenotype:
  Only blonde/blue-eyed child of a blue-eyed/red-haired male and brunette/blue-eyed mother.\n\nSiblings all dark haired


human_id: hu78E4B0
date: 2015-09-24 02:53:22
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  transitioned to a nearly platinum blonde and gradually transitioned through dark shades of blonde until resting at my current brown shade. I am now at the very beginning stages of graying. I'm not sure if this is relevant


human_id: hu776C1D
date: 2015-09-30 01:29:58
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I know I am not 0 and I know I'm Rh negative. But I can't remember whether I'm AB- or just A- or B-.


human_id: hu776C1D
date: 2015-09-30 01:29:58
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  both of my grown children have brown eyes like their father%2C whose mother had blue eyes and father had brown eyes).


human_id: hu776C1D
date: 2015-09-30 01:29:58
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  though I have a sister born with very blonde hair. Now I color it. But it has some graying in it at 53.


human_id: hu646527
date: 2015-10-01 12:33:18
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  so write and do small-muscle activities with my right hand and throw/kick/do large muscle activities with my left hand/side.


human_id: hu3384B3
date: 2015-10-04 20:39:57
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  almost white blonde.  It started to darken slightly each year beginning when I was in elementary school


human_id: hu3384B3
date: 2015-10-04 20:39:57
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  and by the time I was in high school it was a very dark blonde/light brown color.  It has continued to darken slightly and is now a light to medium brown.


human_id: huBADF69
date: 2015-10-05 18:49:03
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  depending on how tired I am depends on how brown or how light brown and green they are. Usually when I am very tired my eyes are dark brown


human_id: huBADF69
date: 2015-10-05 18:49:03
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  When I was younger I had platinum blonde (almost white) hair. But as I grew older it turned into a brown


human_id: huD649F1
date: 2015-10-11 17:58:17
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My eye color now is the same as my eye color at birth. Hazel eyes run in my family for some (not all) family members. \n\n


human_id: huD649F1
date: 2015-10-11 17:58:17
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I was a 'towhead' blonde - nearly white blond as a young child. Then settled to strawberry blond. That's continued


human_id: huD649F1
date: 2015-10-11 17:58:17
phenotype_category: Basic_Phenotypes:Any final thoughts?
phenotype:
  both for congenital cataracts.\n\nMy father had "20:200" vision in that he could see perfectly at 200 feet what a person with 20:20 could see at 20 feet. 'Bird's eye vision.'


human_id: huD22AB8
date: 2015-10-11 21:36:57
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I think my eyes are greener than when I was young.  I have a brown spot next to the pupil of my left eye


human_id: huA38896
date: 2015-10-12 13:17:41
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My moms side of the family has both blue eyes and a tendency toward macular degeneration.  My dads side has brown/green eyes.


human_id: huE11C66
date: 2015-10-12 21:31:37
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  can't remember which. Otherwise his eyes were the same green as mine. Neither I nor my either of my 2 brothers have that. My paternal grandfather had pale neutral gray eyes. My paternal grandmother had brown eyes that were practically black


human_id: huE11C66
date: 2015-10-12 21:31:37
phenotype_category: Basic_Phenotypes:Any final thoughts?
phenotype:
  her daughter and her 3 granchildren had bright red hair. My fathers hair was black and turned red before it turned gray.


human_id: huD59A33
date: 2015-10-13 12:44:41
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  but if you look closer they are similar to eye #14 with a thin ring of gold yellow around the pupil. When I cry or eyes are heavily watered


human_id: hu5917F3
date: 2015-10-13 14:31:45
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  not really blonde or brown.  I put brown on my drivers license but it's a different color from those who are born brown haired


human_id: hu466B05
date: 2015-10-19 19:39:45
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  eyes were darker blue when very young; overall eye blue color is most similar to my father's mother; except for the similar yellow starburst pattern which is very similar to my mothers


human_id: hu466B05
date: 2015-10-19 19:39:45
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  had darkened to a golden blonde before I was 5 and slowly darkened from about age 12 to its current dark blonde color by the time I was 18


human_id: huB1F492
date: 2015-10-20 23:31:58
phenotype_category: Basic_Phenotypes:Left Eye Color - Text Description
phenotype:
  blue/green with a fairly wide and high contrast limbal ring and a tiny bit of yellow around the pupil


human_id: huB1F492
date: 2015-10-20 23:31:58
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  Eye color may have been a bit lighter in childhood. Eye doctors have always commented on my large iris size.


human_id: huB1F492
date: 2015-10-20 23:31:58
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  but is still blonde/red. It typically gets sun bleached in the summer and lightens a shade or two. At age 50


human_id: huB1F492
date: 2015-10-20 23:31:58
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I have only found one grey hair -- maternal size of family does not go grey. My 80-year-old mother has primarily brown hair that is darker than 20 years ago. She has very little grey hair. It is said that my great-grandmother had dark brown hair until her death in her 80s.


human_id: huE9E777
date: 2015-10-21 18:32:39
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  They used to be more blue/green in color. Left pupil is slightly bigger than right pupil.  My eve doctor was concerned that the pupil in my left eye reacted to light slower than my right eye.


human_id: huEAE6C8
date: 2015-10-21 23:09:24
phenotype_category: Basic_Phenotypes:Left Eye Color - Text Description
phenotype:
  Grey/blue ring with black and white lines radiating through blue iris with a small amt of yellowish around the pupil


human_id: huEAE6C8
date: 2015-10-21 23:09:24
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  Very coarse hair that collects a film (no product).  Apparently smells strongly "like hair" and it resists dye.


human_id: hu3D46CB
date: 2015-10-24 13:02:47
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  but can write with my left hand as well as many people write with their right hand. So "both but not equally well".


human_id: hu3D46CB
date: 2015-10-24 13:02:47
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  and I got his eyes. My sister's eyes are a bit lighter and so are my kids' (their father is Central Asian with brown eyes but green eyes in his family).


human_id: hu3D46CB
date: 2015-10-24 13:02:47
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My mother's hair turned brown after she had her first baby. Apparently that's common on her father's side. But I took after my father so my hair was black all the way through.


human_id: hu52F6FF
date: 2015-11-11 20:08:15
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I had light blonde hair. It became darker around age 7 or so. It's still lighter than either of my parents' hair. When my hair is exposed to sunlight


human_id: hu6F6F6C
date: 2015-11-12 19:05:25
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  Father with legal blindness from macular degeneration. There is a history of blindness in men in his genealogy with unknown cause.


human_id: hu6F6F6C
date: 2015-11-12 19:05:25
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  Born with black hair that fell out and was replaced with light brown hair that darkened at about age 12 and then started graying about age 39


human_id: hu925B56
date: 2015-11-13 08:32:48
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My hair was nearly gold until I was 5. It slowly darkened to medium-dark brunette with reddish-gold (more gold than reddish) highlights until I found my first grey hair on my 18th birthday. My family does not normally grey early


human_id: hu91ACB9
date: 2015-11-22 21:55:38
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  Siblings (2 brothers%2C 2 sisters) all have brown or hazel eyes\nFather had brown eyes\nMother had blue eyes


human_id: huEFD66A
date: 2015-11-30 13:46:06
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  all of my dad's offspring and their children have blue eyes - including a set of half black half white twins.


human_id: hu5D0BAB
date: 2015-12-01 22:18:54
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My hair was sandy brown when I was a young child and darkened to its current color by the time I was in school.


human_id: huAF3C63
date: 2015-12-02 13:19:22
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  In case this is useful:\n\n- I was diagnosed with endometriosis when my daughter was born via c-section in Sept 2005. ObGyn removed what she could and reported no signs or endometriosis when my son was born in April 2008 via c-section. Both of my kids were breech babies.\n\n- I am the only one of 4 siblings not using glasses. My 3 siblings had had some eye surgery and wore glasses by the time they were 5 years old\n


human_id: huF33303
date: 2015-12-10 23:51:06
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  All of my family has blue eyes. My eyes are about the same color as they were at birth. All of my family wears corrective lenses except me.


human_id: huB4E868
date: 2015-12-15 14:37:51
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My eyes are pretty much all brown and appear to have been the same color since I was a child. There is no history of eye disease in my family. My mother has brown eyes and my father has blue eyes.


human_id: huE02FAC
date: 2015-12-18 17:39:35
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I'm balding now.  The hair on my scalp is much softer than the hair in my beard.  I have multiple colors of hair in my beard as well


human_id: hu6BF6F9
date: 2016-01-03 17:59:58
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  eyes at birth were dark blue as all babies are. astigmatism in my eye.\nfamily hx of glaucoma.  family hx of nearsightedness\n\ncolor #11


human_id: huA5B645
date: 2016-01-04 20:36:31
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My eyes change color from pale blue-gray to rich ocean blue to full green depending on ... clothes? emotional state? energy level? I can't say for sure.


human_id: huA5B645
date: 2016-01-04 20:36:31
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  when it became light brown which turned darker over the next 10 years. This pattern holds true with my 5 siblings (black -> blond -> brown). The younger three siblings kept their blond hair to various degrees


human_id: huCB92AC
date: 2016-01-05 21:59:45
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  This is a recessive color in my family - same as my maternal grandmother. Both of my parents and all of my siblings have brown eyes.  My niece also has the same color eyes as me.  I have CHRPEs in both eyes


human_id: hu0C8573
date: 2016-01-05 23:03:37
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I mean my eyes are pretty normal. I have two of them. They're nice and dark. I use them to see. I also use them to wink at the ladies. My immediate family also has dark brown eyes


human_id: hu0C8573
date: 2016-01-05 23:03:37
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  but then it came to its senses during my childhood. My hair gets lighter when I spend a lot of time in the sun


human_id: hu0C8573
date: 2016-01-05 23:03:37
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  so I shave the sides of my head and keep the top just long enough to look damn good. My head gets super hot when I don't cut it at least once a week. I use Wahl clippers. Wahl is a good brand. Unfortunately I know of no brand of pillows that stay cool for when I forget to cut my hair.


human_id: hu0C0779
date: 2016-01-06 02:47:08
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I'm usually 10lbs heavier but after I had baby baseline weight shifted down 10lbs and nicotine use (15+ mg total via oral tablets daily) has kept it there.


human_id: hu0C0779
date: 2016-01-06 02:47:08
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  One upper eyelid folds more than other. Makes one eye shape more round than other when eyes are open.


human_id: huE35226
date: 2016-01-06 03:19:00
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I also write poorly with both hands.  A few people seeing my right handed writing at first thought I was left handed based on it and the usual deformities and discrepancies they see in their own off-handed writing.  My left hand writing is worse (and the same distortions "discrepancies" the previous individuals pointed out to me are indeed stronger there) but I am not sure if that is just the difference in practice or not.


human_id: huE35226
date: 2016-01-06 03:19:00
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I took a few image closeups of my eyes with a good camera ... but I am really having a hard time distinguishing between 1–4 on your iris color chart!  I think I am as blue as 1


human_id: huE35226
date: 2016-01-06 03:19:00
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  but I have some of those extremely small and faint "browner" coloration bits like some of the later ones.


human_id: huE35226
date: 2016-01-06 03:19:00
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  Hair color has shifted over my lifetime just like my father.  I started life platinum blonde and was pretty intensely blonde until my early teens


human_id: huE35226
date: 2016-01-06 03:19:00
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I have been browning ever since and some people don't think I am blond at all any more.  I presume I am on the same path as my father


human_id: huD8A898
date: 2016-01-06 13:14:18
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  but it was deemed likely that the impression was due to my rarely having my eyes wide open.  I have not looked at old photos to verify the impression.


human_id: hu919BE3
date: 2016-01-06 16:15:46
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My eyes have always been a deep blue. Looking closely for this survey I can see a very small amount of hazel near the iris. Both my brother and I have blue eyes


human_id: huB19789
date: 2016-01-06 19:29:09
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I was naturally left handed as a small child but my grandmother thought that it would negatively affect me so she always had me use my right hand. This created a coordination problem for me which was discovered when I was 6 when I was diagnosed with Developmental Coordination Disorder.


human_id: hu5A306E
date: 2016-01-08 15:23:26
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I am told that everyone in my family is born with blue eyes. I thought for some reason that all babies were.


human_id: huD09534
date: 2016-01-10 17:41:18
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  Maybe I'm silly but my eyes are greener than anything I see above.  There is definitely a brown center like 14 & 15 but the color around it is as hazel/moss greenish as it could be.


human_id: hu27340D
date: 2016-01-12 10:05:11
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I am functionally left handed (even though I write with the right after being forced in school to switch hands for writing back)


human_id: hu46528F
date: 2016-01-13 12:21:17
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  it is thinning some now @ 67 and not gone grey  but lost much of its color which makes it look light blond almost platinum


human_id: hu46528F
date: 2016-01-13 12:21:17
phenotype_category: Basic_Phenotypes:Any final thoughts?
phenotype:
  their eyes were brown or lighter brown than mine.  They were all taller than me.   I suspect that I am somewhat colorblind in the blue-brown-green category


human_id: hu77C5CB
date: 2016-01-13 12:43:31
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I was born with white hair and it turned to a dishwater blonde as I aged and now it has gone back to being mostly white.


human_id: hu77C5CB
date: 2016-01-13 12:43:31
phenotype_category: Basic_Phenotypes:Any final thoughts?
phenotype:
  My maternal grandfather's hair turned white early in his life as well.  I'm not sure what color his eyes were.  He was of German descent.


human_id: hu08334F
date: 2016-01-13 15:06:01
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  Eyes in my family run in the blue to green range.  Kids (including me) often start out more blue and then darken somewhat as they grow up.


human_id: hu08334F
date: 2016-01-13 15:06:01
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  mother has red hair.  My hair is medium brown and started graying in my 20's.  Now I'm about 25% gray (at age 50).  My beard is also brown but shows a much stronger red tone to it with some individual hairs appearing quite reddish.


human_id: hu6664F3
date: 2016-01-21 16:34:48
phenotype_category: Basic_Phenotypes:Any final thoughts?
phenotype:
  Several genetic linked traits\ntongue rolling-yes\narm folding- left hand on top\nhand clasping- left thumb on top


human_id: hu453E0E
date: 2016-01-28 23:08:50
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My eyes did not turn green until about the age of 18 months. They were blue prior. My maternal grandmother had the same color eyes and my daughter has them


human_id: hu453E0E
date: 2016-01-28 23:08:50
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I was born with very blonde hair which turned to dark blonde during puberty around the age of 11. It has gotten darker since and is now turning gray.


human_id: hu73BFBC
date: 2016-02-01 16:37:13
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My eyes were blue through my childhood and gradually turned more green through my teenage years. My eye color changes when I am sick


human_id: hu329CC4
date: 2016-02-01 21:02:28
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  Eyes are less blue than they were as a child. Blue eyes common in family.  Retinal detachment and macular degeneration common in family history.


human_id: hu43294F
date: 2016-02-04 15:46:18
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My eyes were light blue when I was young. They have since developed into a greenish-blue and in certain circumstances they change colors from either light blue


human_id: hu43294F
date: 2016-02-04 15:46:18
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My hair has always been dark brown...in the sun it will get slightly blonde on the ends and in the front. It also has a tendancy to look a little bit redish.


human_id: hu9E8595
date: 2016-02-07 23:54:54
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  born with dark brown hair. texture was thick. at senior stage still have most of my hair. very fast growth.


human_id: hu9E8595
date: 2016-02-07 23:54:54
phenotype_category: Basic_Phenotypes:Any final thoughts?
phenotype:
  able to maintain physical fitness with minimal efforts. broad chest with narrow waist when younger led to difficulty buying jackets and business suits.


human_id: huF6B0B1
date: 2016-02-16 16:29:11
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I naturally have somewhat pronounced dark blonde highlights throughout my hair. My hair had much more red in it and was a little straighter when I was younger. My hair is very thick and curly. I have hair similar to my dad


human_id: huF6B0B1
date: 2016-02-16 16:29:11
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  and he didn't start getting gray hair until his mid 50s. He is now in his mid 60s and his hair is still about 85% brown with no pattern baldness. My paternal grandfather was the same way.


human_id: hu54EEB2
date: 2016-02-16 18:34:32
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I shoot pool left handed. I don't know why. It is the only thing I do left handed. I am pretty good at it too!


human_id: huF9F779
date: 2016-02-23 18:50:31
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  a green outer ring can be observed in both eyes.  Left eye has dark brown flecks in outer ring.  My mother had hazel eyes


human_id: huF33837
date: 2016-02-26 17:16:37
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  born very light blonde. hair darkened with puberty and became light brown or dark blonde with gold and red highlights


human_id: hu36A660
date: 2016-03-08 15:35:15
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  so I assume there are flecks of multiple different colors in them.  I had corrective (lasik) surgery when I was 27; prior to that my right (dominant) eye was 20/400 vision


human_id: hu7A2F1D
date: 2016-03-18 19:38:02
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I was born with blond hair that turned to brown and started turning gray in my 50s and white in my 60s. My eyebrows are still brown but turning gray.


human_id: huDAA62E
date: 2016-04-08 20:33:24
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  it's been light brown since then.\n\nMy hair also has two natural red highlights that grow at my temples.


human_id: huFF6AB4
date: 2016-04-12 15:55:38
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My eye color changes from green to blue over the course of a month.  The blue can be an icy clear blue with very few flecks.  The green can be smooth moss color (like today) or flecked with amber.    Others have commented on the way my eye color changes


human_id: huFF6AB4
date: 2016-04-12 15:55:38
phenotype_category: Basic_Phenotypes:Any final thoughts?
phenotype:
  The full page eye images at Google is no longer working.  The distinction between the top 3 rows of examples is very hard to see


human_id: huFF6AB4
date: 2016-04-12 15:55:38
phenotype_category: Basic_Phenotypes:Any final thoughts?
phenotype:
  leaving much uncertainty in my answer.   And I see no examples with clear moss green.\n\nHave you considered having participants submit a photo of their eyes so you could draw the more subtle distinctions needed?   Closeup selfies could maintain confidentiality while giving you higher quality input. \n\nOverall


human_id: hu01EECF
date: 2016-04-12 16:59:50
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My natural hair color is a dark golden blonde. Depending on the season it looks darker brown or dark blonde with yellow highlights.


human_id: huA3177D
date: 2016-04-12 18:21:01
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I used to be told my eyes were hazel.  But they were bluer when I was born and growing up than they are now.


human_id: huA3177D
date: 2016-04-12 18:21:01
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I was born with very light colored hair.  My mom used to say it was white.\nLater it turned blonde and darkened as an adult.


human_id: hu0B4653
date: 2016-04-24 21:39:27
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My mom had to have cataracts surgery.\nEveryone in my family has glasses and my sister is legally blind without corrective lenses because her vision is so bad.


human_id: hu0B4653
date: 2016-04-24 21:39:27
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My hair was white-blonde when I was born.\nMy hair is currently dyed red but my natural color is blonde.


human_id: hu0B4653
date: 2016-04-24 21:39:27
phenotype_category: Basic_Phenotypes:Any final thoughts?
phenotype:
  I have a good amount of freckles on my face and around my body but my mom is covered in so many freckles that I like to say she doesn't tan


human_id: hu82AAD7
date: 2016-04-26 11:34:46
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I would say that my hair is now darker than when I was a toddler (post-chemotherapy). If my hair starts to get long


human_id: hu82AAD7
date: 2016-04-26 11:34:46
phenotype_category: Basic_Phenotypes:Any final thoughts?
phenotype:
  the colors in the iris color chart are too close together. It was also confusing at first glance because of the tiny white circles on the pupils. I knew the iris was the colored part


human_id: hu82AAD7
date: 2016-04-26 11:34:46
phenotype_category: Basic_Phenotypes:Any final thoughts?
phenotype:
  but decided to do a quick web search just to double-check what the iris was (the white circles made it seem like you wanted the color of the pupil%2C which doesn't make sense).


human_id: hu02C8E3
date: 2016-05-03 14:13:33
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I write with my right hand but can do a lot of things (including drawing) with my left hand. My mother was left-handed.


human_id: hu02C8E3
date: 2016-05-03 14:13:33
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  color blindness in different degrees runs in men on my father's side; my brother can't distinguish some shades of pink


human_id: hu609D1E
date: 2016-05-20 18:03:58
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  but it gradually turned brown as I grew up. Upper half of beard still comes in a mixture of blonde and brown. Lower half is completely brown.


human_id: hu609D1E
date: 2016-05-20 18:06:05
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I was born with dirty blondish hair that gradually turned brown as I grew up. Mustache and cheeks come in partially blonde while rest of the beard comes in brown.


human_id: hu5E8E50
date: 2016-06-04 19:22:36
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My weight can fluctuate between ~135 and 155 depending on my level of activity and eating habits at the time.


human_id: hu81BCA8
date: 2016-06-10 12:57:21
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My father/mother/brother all have green eyes.  I have blue.  My maternal grandmother had brown eyes.


human_id: hu81BCA8
date: 2016-06-10 12:57:21
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  Born with black hair that fell out and came back the lightest blonde.\nProgressively got darker through childhood and into adulthood.


human_id: hu955EE1
date: 2016-06-10 17:30:49
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My hair has gone white on the sides of my head. (All the males on my father's side of the family eventuallly go completely white.) On the top it is a mix of white and light brown hair.\n\nWhen I was younger


human_id: hu955EE1
date: 2016-06-10 17:30:49
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  (especially in my beard) there was always a number of black hairs and the occasional red hair interspersed with the light brown.\n


human_id: hu868880
date: 2016-06-20 12:14:16
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  my father was left handed and I have some measure of comfort doing things with my opposite hand. In addition what is believed to be a congenital brain injury (AVM) in the left parietal lobe may have resulted in the migration of certain functions to the opposite lobe (hypothesis by neuropsychologist at Brown University after work up in the early '90s)


human_id: hu868880
date: 2016-06-20 12:14:16
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  photos from my childhood show my hair was very blond and it was often described to me as 'strawberry blonde'... as i've gotten older it has gotten darker. my eyebrows are very blonde


human_id: hu64A49C
date: 2016-06-28 18:03:37
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  very light blonde (almost light yellow/white) as a child - started to change to dusty/dirty blonde during adolescence and color has remained the same throughout adulthood


human_id: hu5A38F5
date: 2016-07-08 12:59:09
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  THE GREEN IN MY EYES IS SOMETIMES MORE VISIBLE THEN OTHERS THE BLUE HOWEVER IS THE MAIN COLOR OF MY EYES AND IS WHAT IS ON MY I.D. AND BIRTH CERTIFICATE


human_id: hu4EEA9B
date: 2016-07-27 11:33:03
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  yet things such as martial arts put me on a path to learning how to be equal with both hands and feet.  I am left-eye dominant


human_id: hu4EEA9B
date: 2016-07-27 11:33:03
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I can do it very well with either hand.  I can also use my feet very well.  I am extremely physically capable and fast.  My eye color is hazel


human_id: hu4EEA9B
date: 2016-07-27 11:33:03
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  with a dark ring around the edge.  My eyes were blue until shortly after five years of age.  My hair used to be lighter


human_id: hu4EEA9B
date: 2016-07-27 11:33:03
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I have double cowlicks on the crown of my head.  My hair has always been very thin/fine.  It is relatively straight


human_id: hu4EEA9B
date: 2016-07-29 19:22:19
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  and all limbs for just about anything.  I am extremely well-talented with using my physical capabilities


human_id: hu4EEA9B
date: 2016-07-29 19:22:19
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  Perfect vision if that's relevant to this survey.  Eyes used to be blue until shortly after age five.  I am left-eye dominant.


human_id: hu4EEA9B
date: 2016-07-29 19:22:19
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  the color began to darken.  I have several strands that are different colors.  From some that have been blonde in appearance


human_id: hu4EEA9B
date: 2016-07-29 19:22:19
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  and is likely because of my lack of being hairy.  Perhaps some research into that subject would benefit science.  Hairy creatures generally have to pant to relieve body heat due to lack of sweat glands


human_id: huDBDF82
date: 2016-07-29 21:04:27
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I had brown hair. First whites in grade school.  White stripe by graduate school.  Almost all white at 40


human_id: huDBDF82
date: 2016-07-29 21:10:45
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I had dark brown hair starting  to get white in high school.  By graduate school I had a white streak in front.  Almost all white by 40.


human_id: hu1C3ACB
date: 2016-08-07 06:49:09
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  Hair dark brown at birth. Had a red tint during preschool ages. Turned dark brown by school age & has not changed color.


human_id: hu4623CD
date: 2016-08-13 12:14:10
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I have always considered my eyes black because it is often hard to discern the pupil. They seem lighter though than my youth.


human_id: huFB4F9E
date: 2016-08-19 09:41:05
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  As I've gotten older my eye color as slightly lightened and become barely noticeably less of the vibrant ocean teal color and a bit more on just the deep blue side. It's actually one of my features that people comment on the most often.


human_id: huFB4F9E
date: 2016-08-19 09:41:05
phenotype_category: Basic_Phenotypes:Hair Color - Text Description
phenotype:
  darker at the roots where it's a light auburn brown and the more it's exposed to sun the lighter it gets


human_id: huFB4F9E
date: 2016-08-19 09:41:05
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I was born with very red hair and it stayed that way until about puberty. Afterwards it was a medium blonde for years until I started having my 4 kids


human_id: hu37161B
date: 2016-09-04 16:29:00
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My hairline seemed to recede an inch or less at about age 18 and not much since that time.  I still have most of my hair.


human_id: huDD5D00
date: 2016-09-05 12:18:18
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  Was much darker when I was younger - almost black. Now it seems to be a lighter hue of dark brown and I'm finding a few white hairs already (probably due to stress).


human_id: huDD5D00
date: 2016-09-05 12:18:18
phenotype_category: Basic_Phenotypes:Any final thoughts?
phenotype:
  I'm just very interested in how my eye and hair color have changed over time. I've never really known what to call my eye color. It gives me pause on a questionnaire.


human_id: huBE7BAD
date: 2016-09-09 14:14:07
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  my eye color is way different than it was when I was little. my eyes were pale blue until I was in around 3rd grade. then they still were kind of grey for years and only in my teens some orange came in. in my twenties they started hazel and gradually got to the muted green they are now at 35. they both still have some orange


human_id: huBE7BAD
date: 2016-09-09 14:14:07
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  more noticeably in my right eye than my left. lots of people still describe my eyes as blue but they don't look blue at all up close.  \n\nmy dad has weird grey eyes. I don't know what his looked like when he was young


human_id: huBE7BAD
date: 2016-09-09 14:14:07
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  but my daughter was born with pale blue eyes like me and they darkened as she aged. she's 16 now and her eyes look exactly like my dad's eyes. it's a kind of grey that almost doesnt seem like a real color when you look right at it. kind of a dull steel-ish color that looks different depending on the surroundings. like seeing silverware at the bottom of a creek.\n\nmy dad has one eye that rolls sideways


human_id: huBE7BAD
date: 2016-09-09 14:14:07
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  and my daughter has permanent double vision and no depth perception because her eyes both roll away from each other.  the doctor said her brain would delete one eye but it never did. \n\nmy daughter was diagnosed with "retinal migraines" in addition to her eye roll. she was also born pretty strongly farsighted. my dad wears a super strong prescription as well but I don't know his specifics.\n\nmy left eye doesn't close all the way and I have to cover it when I sleep


human_id: huBE7BAD
date: 2016-09-09 14:14:07
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  but I think that's from an injury. \n\nmy daughter didn't open her eyes at all for the first six weeks or so after she was born and then she slept with her eyes completely open every night until she was about 15 months old.\n\nmy daughter and I definitely see colors differently but I don't know which of us has any colorblindness.


human_id: huBE7BAD
date: 2016-09-09 14:14:07
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  my hair was light blonde until I was 7 or 8. then people described it as "dirty blonde" for a lot of years


human_id: huBE7BAD
date: 2016-09-09 14:14:07
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  and now it's unambiguously just brown. I have some streaks that showed dark when my hair was light and showed light when my hair got darker


human_id: huBE7BAD
date: 2016-09-09 14:14:07
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  but i think the streaks were always the same color. they were visible enough on my scalp when i was an infant that hospital staff thought it was vernix and tried to scrub them off. when i shaved my head in my teens i could still see the stripes on my head


human_id: huBE7BAD
date: 2016-09-09 14:14:07
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  but when i shaved it this summer I couldn't see them. I do still get asked if I bleached highlights in even though I can't find the blonde streaks when i look in the mirror.\n\nmy beard is a mix of brown


human_id: huBE7BAD
date: 2016-09-09 14:14:07
phenotype_category: Basic_Phenotypes:Any final thoughts?
phenotype:
  my dad's hair went from black to completely white in his early thirties. he looked like steve martin. i have more silver hairs than other thirtysomethings I know but nothing like my dad.\n\ni am the only one i've met in my immediate or extended family to have hair like mine. my mom and sister have dark brown curly hair with dark brown eyes and my brother has bright red curly hair with light green eyes. all my mom's family I've met have either black or red hair or it's gone white and I don't know what color it used to be. my dad's side is all dark brown and black and they all seem to have blue or grey eyes.


human_id: huE0E689
date: 2016-09-19 16:08:39
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I was told about two and a half years ago by an opthamologist that my lenses are having trouble focusing. Over time


human_id: huC3ACB0
date: 2016-09-27 21:41:56
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  Eyes are currently a lighter shade of blue than they were at birth. Nearsighted. Contact prescription is left eye -2.75 right eye -3.00. Right eye has been consistently far more near sighted than left eye


human_id: hu652406
date: 2016-09-29 16:46:57
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  Color is lighter now than as a child. History of very dark blue and green eyes run on both sides of the family.


human_id: hu60431C
date: 2016-10-04 02:48:52
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  less than 9 months noticed\n\nhave seen slightly different colors in eyes for as long as can remember\n(slightly warmer colors in right (red yellow orange) and more blue green in left). right maybe more contrasted and saturated


human_id: hu60AB7C
date: 2016-10-11 18:36:46
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My eyes seem to have changed from solid brown to this ringed design.  I have the bad habit of sleeping with my right eye buried in my pillow and this has distorted my cornea


human_id: hu60AB7C
date: 2016-10-11 18:36:46
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  much to the chagrin of laser surgeons trying to correct it permanently.  My mother's eyes changed from brown to ringed grey


human_id: hu60AB7C
date: 2016-10-11 18:36:46
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  and he was several times legally blind from near nearsightedness.  The older of my two younger sisters was born with grey eyes which became ringed


human_id: hu60AB7C
date: 2016-10-11 18:36:46
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  and then solid crystal blue.  My youngest sister always had solid crystal blue eyes.  My Paternal Grandmother's eyes changed from my color to crystal blue very late in life.  My paternal grandfather had solid medium brown eyes and nearsightedness.  My Maternal Grandparents had crystal blue eyes.  My Paternal male cousin has medium brown eyes(mild late age farsightedness)


human_id: hu60AB7C
date: 2016-10-11 18:36:46
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My hair seems to have come from my mother who also had very thin hair strands.  Both my Mother and Paternal Grandmother seem to have suffered from a degree of mercury poisoning from Gamma 2 Amalgam fillings.  My paternal grandmother suffered from what appeared to be the uniform loss of about 2/3 of her hair


human_id: hu60AB7C
date: 2016-10-11 18:36:46
phenotype_category: Basic_Phenotypes:Any final thoughts?
phenotype:
  or oils.  In my 40's when I tried to supplement with them I became very agitated.  After finishing the a pint of Hemp Oil at about a tablespoon a day


human_id: hu60AB7C
date: 2016-10-11 18:36:46
phenotype_category: Basic_Phenotypes:Any final thoughts?
phenotype:
  my skin changed.  Suddenly many of the scars from my childhood became LIGHT colored on my tanned hands.  On the tip of my pale penis an unseen scar became DARK colored.  After using a tanning bed several times across a couple of weeks during the 80's certain dark scars/moles began to change color and shape appreciably.  None of the scars/moles exposed to constant sunlight or not all year round


human_id: hu60AB7C
date: 2016-10-11 18:36:46
phenotype_category: Basic_Phenotypes:Any final thoughts?
phenotype:
  displayed any changes.  My Paternal Grandfather died of a cancerous mole on his back.  My Paternal Grandmother had "liver spots" all over her hands.  My Maternal Grandfather had a skin condition which made the capillaries in his face pronounced


human_id: hu60AB7C
date: 2016-10-11 18:36:46
phenotype_category: Basic_Phenotypes:Any final thoughts?
phenotype:
  and my mother developed this in later life.  My Maternal grandmother did not have this. Both me and my father have had "wax pockets" or clogged pores which have filled with so much wax


human_id: hu60AB7C
date: 2016-10-11 18:36:46
phenotype_category: Basic_Phenotypes:Any final thoughts?
phenotype:
  or emptied.  My sisters and mother did not have this.  Surgeons have told me that I heal remarkably fast


human_id: hu70ED6F
date: 2016-10-18 01:12:49
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  green around edges; appear brown overall but are actually mostly green.\n\nAlways thought my eyes were just different shades of brown (as in photo 20)


human_id: hu70ED6F
date: 2016-10-18 01:12:49
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  they seem to have gradually become more and more green.\n\nMy mother have brown eyes (closest to photo 21) and my dad has blue eyes (closest to photo 4). My brother


human_id: hu70ED6F
date: 2016-10-18 01:12:49
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I was a hairstylist for over 8 years. Peoples' hair tends to become darker as they age from childhood to adulthood. Mine


human_id: hu70ED6F
date: 2016-10-18 01:12:49
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  it became lighter with ash undertones until it became dark blonde with natural blonde highlights. I have never


human_id: hu70ED6F
date: 2016-10-18 01:20:49
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  hair began to lighten from dark chocolate brown (level 4 w/red undertones) as I began puberty until it became current color (has some natural blonde highlights) \n\nI was a professional hairstylist for over 8 years and have NEVER seen this


human_id: hu70ED6F
date: 2016-10-18 01:20:49
phenotype_category: Basic_Phenotypes:Any final thoughts?
phenotype:
  Very curious about eye and hair color.\n\nForgot to mention mother has VERY dark brown hair (almost black; level 2.5) and dad has light ash blonde hair (level 10)


human_id: huD82893
date: 2016-11-12 21:58:42
phenotype_category: Basic_Phenotypes:Hair Color - Text Description
phenotype:
  but I am starting to go gray/white so there are a few strands of that here and there. (Hair dye to the rescue!!)


human_id: hu8DFB85
date: 2016-12-02 15:47:30
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I had blue eyes as a young child. They were green by the age of 13.\n\nMy father and brother had blue eyes; my mother


human_id: huBF974E
date: 2016-12-02 16:50:22
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My hair was very dark brown at birth and gradually got lighter.  Medium brown in elementary school/middle school to light brown later in high school and onward.


human_id: hu498BDE
date: 2016-12-06 19:07:27
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  mother approx 5'6".  There are no members of my nuclear or extended family who exhibit this unusual stature.


human_id: huEC83E7
date: 2016-12-07 17:34:38
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  When I was born I had very little and it was white.  As I got older it became more of a golden blonde.  After I had children it got increasingly darker to the dirty blonde it is now.


human_id: hu6B7829
date: 2016-12-11 20:15:46
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  The intensity of the blue-ness of my eyes can change from day to day.  Some days they may appear more gray or have shards of hazel.  Usually they are distinctly blue


human_id: hu6B7829
date: 2016-12-11 20:15:46
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I have some gray now.  My hair looses its color very easily so the color at the roots is usually darker than farther down the shaft even if not color treated.


human_id: huFE1782
date: 2017-01-18 00:47:32
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  darker then when i was born. hair was very much lighter blond and very straight has more waive not much but still baby fine


human_id: hu5CA053
date: 2017-01-30 11:34:25
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I was born with dark brown eyes but as an adult they've changed. I appear to have central heterochromia in both eyes now and they are mostly green


human_id: hu1DC288
date: 2017-02-01 03:27:17
phenotype_category: Basic_Phenotypes:Left Eye Color - Text Description
phenotype:
  Electric blue with a sapphire blue ring on the putter iris and a dark blue almost black ring around the pupil


human_id: hu1DC288
date: 2017-02-01 03:27:17
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  Eye color has basically been the same since birth. Majority of family members have vision problems requiring corrective help ie; glasses and contacts


human_id: hu1DC288
date: 2017-02-01 03:27:17
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  which was curly/ringlets. After a major cut it became all over wavy with extra curly areas. Hair is more porous like African-American hair rather than Caucasian.


human_id: huB06CDB
date: 2017-02-14 12:31:28
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  Had astigmatism \nPredominant family members have brown eyes \nNot the same blue tones as either parent\nLarge eyes\nDidn't note stripes (from the center outward) until approximately 18y/o\n


human_id: hu8FCC8F
date: 2017-02-26 13:01:18
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  The green is rarely presented but when it is it is in flecks around the center only.  The color blue runs in my father's family


human_id: hu8FCC8F
date: 2017-02-26 13:01:18
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  while blue/blue-green runs in my mothers.  Some people in my family (both sides) have brown eyes but are born with dark blue at first and by the age of two or sometimes sooner they turn brown.


human_id: hu8FCC8F
date: 2017-02-26 13:01:18
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  so white that the first two years of my life I looked bald.  Then come puberty my hair started to darken until the color it is today.  This is very common on my mothers side of the family.  Her and her four siblings were born with white hair and today my mother and the surviving siblings have dark brown hair.


human_id: huD7DB72
date: 2017-03-10 19:51:39
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My mother always said I had blue eyes until she looked at them (a second time?!) when I was about 10. I am the only one in my birth family who does not have pure blue eyes. All four of my children have blue eyes. A granddaughter has green eyes but her father (my son-in-law) does


human_id: huD7DB72
date: 2017-03-10 19:51:39
phenotype_category: Basic_Phenotypes:Any final thoughts?
phenotype:
  I think it is interesting how children inherit parents' traits regardless of sex. I have my father's square hands


human_id: huD7DB72
date: 2017-03-10 19:51:39
phenotype_category: Basic_Phenotypes:Any final thoughts?
phenotype:
  for example. My husband has delicate features for a man and I have much stronger features fora woman. Our four children are  mixtures of both their parents


human_id: hu7F50FF
date: 2017-03-13 15:53:21
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  green (no brown); has always been this color; all 3 siblings and parents had the same color; daughter has the same color; son has grey eyes.


human_id: hu9AF15C
date: 2017-03-15 15:25:45
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  now my eyes are blueish green gray and change color depending on what I am wearing and what the weather is like- sometimes they appear more gray - sometimes more blue


human_id: huA80B79
date: 2017-03-15 15:38:11
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My hair color as a child would go from shock white in the summer to a dark dirty blond in the winter


human_id: hu4B6D1D
date: 2017-03-17 13:18:18
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  Height varies with spinal compression over the course of the day. Usually tallest when measured immediately after a night's sleep.


human_id: hu4B6D1D
date: 2017-03-17 13:18:18
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  becoming progressively greener with fluctuations through teens and adding hints of brown in late teens/early adulthood. Parents both had brown hazel eyes


human_id: hu4B6D1D
date: 2017-03-17 13:18:18
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  and paternal grandfather had hazel eyes.  Each of my siblings has a different eye color in the range from very blue to brown hazel.


human_id: hu4B6D1D
date: 2017-03-17 13:18:18
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  the individual hairs are a mix of shades. This includes some light blonde hairs and black hairs.  My mustache grows in blonde and dark brown


human_id: hu4B6D1D
date: 2017-03-17 13:18:18
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  with some hairs alternating color as they grow. Though my father had blonde hair as a baby that darkened to brown in adulthood


human_id: hu4B6D1D
date: 2017-03-17 13:18:18
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  my hair has only darkened from mid-range brown to a darker brown. My mother's natural hair before greying and coloring was a very dark brown but without warm tones. I have two small spots of a few white hairs growing together. These have appeared over the last 6 years.


human_id: hu88370B
date: 2017-04-19 23:18:35
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My eyes are blue with green on the inside. One eye has reddish brown speck in it. They used to be completely blue with the one speck. The green on the inside has appeared in the last year.


human_id: hu6C4BCF
date: 2017-04-21 18:33:50
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  but my hair has no indications of carrying that recessive gene. One of my brothers has noticable red highlights in his brown hair.


human_id: hu98F189
date: 2017-04-21 18:51:35
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  Father had Blue eyes\nMother's were hazel (yellow brown)\nI was born with a congenital cataract and at 50yo have had replacement lens due congenital cataract and severe myopia.


human_id: huA33758
date: 2017-04-21 19:16:08
phenotype_category: Basic_Phenotypes:Left Eye Color - Text Description
phenotype:
  My colour division isn't quite as crisp as the pic. My Color is like a burnt amber surrounded by olive.


human_id: huA33758
date: 2017-04-21 19:16:08
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My sister's division between colour rings is more crisp than mine. Our father had ice-blue eyes. Our mother's father had dark blue eyes


human_id: hu7DE7FD
date: 2017-04-21 21:17:12
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  Natural hair color. Very late greying (only a few grey hairs at 48). Rest of my female relatives turned grey in their 30s.


human_id: hu51B2DF
date: 2017-04-21 21:33:58
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My mom thinks I should have been left handed.  I eat left-handed and throw a frisbee lefthanded.  I use chopsticks right handed.  I learned most sports and writing right-handed.


human_id: hu51B2DF
date: 2017-04-21 21:33:58
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  Hair was very light blonde when I was younger and darkened as I got older.  It is almost pushing a light brown/dark blonde at this point with the occasional speck of gray.


human_id: hu5CABA7
date: 2017-04-21 23:04:26
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  Hair in my youth was very dark brown and started going grey at the temples in my early 20s. I was probably more gray than brown by the time I was 40. I don't expect I will go fully gray until around 60 or so


human_id: hu72076D
date: 2017-04-21 23:20:43
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  the same color as my father's hair. It fell out within the first couple of months and came back in white blonde.


human_id: hu7A03F2
date: 2017-04-21 23:23:20
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My eye color was difficult to match to the samples. My mother has Macular degeneration. People remarked on the color of my eyes when I was younger.


human_id: hu6D1115
date: 2017-04-21 23:38:36
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  18 was my first choice. Then I looked again. I might choose differently in a different light. My father has brown eyes. Both his parents had brown eyes. My mother's eyes were blue gray. Her father's eyes were gray


human_id: hu6D1115
date: 2017-04-21 23:38:36
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  it would sunbleach to blonde. When I had long hair in my late teens and 20s-30s I had sunbleached streaks and natural red highlights. I really miss my natural hair color (s). I considered my hair my best feature. I'm heterogeneous for the recessive red haired gene.


human_id: hu6E7E5D
date: 2017-04-22 00:08:26
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  Much more blue eyes at birth.  My brother has one blue eye and other eye almost entirely brown.  No serious family diseases I am aware of.


human_id: hu4D906B
date: 2017-04-22 01:05:51
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  Yes my eyes were a solid blue color until puberty and pregnancy at 16 then they turned colors and my son born from that pregnancy eyes did the same thing


human_id: hu1F7A7D
date: 2017-04-22 01:21:01
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  almost not visible until about the age of 3 and darkened until 13 when it became the dirty ash blonde color it is now.


human_id: hu1097B2
date: 2017-04-22 10:02:50
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  As newborn I had red hair.  It all fell out and grew in wispy white.  Stood on end and I looked like a baby chick.


human_id: hu1F73AB
date: 2017-04-22 12:34:23
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I was discouraged from using my left hand to feed myself when I was 2 years old. Perhaps I was naturally left-handed.


human_id: hu420F49
date: 2017-04-23 23:08:02
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  full-size image: https://goo.gl/XQ2Voh: \n404: Page not found – the page https://goo.gl/XQ2Voh does not exist.\nBut I googled and found it independently.


human_id: huEFD2F0
date: 2017-04-24 09:48:53
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  Very thick until late 20's currently fairly fine and straight. There was a period where it was very curly in my late 40's for about 2 years then went straight again.


human_id: hu10D938
date: 2017-04-25 11:35:03
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  and my dad has very dark blue eyes (like the ocean). The outer ring of my eyes are a combination of theirs


human_id: hu10D938
date: 2017-04-25 11:35:03
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  but I have an inner ring of gold that people find striking against the blue--so striking that strangers stop me in grocery stores or on the street and compliment me on my eyes! My eyes look most similar to #11 in appearance


human_id: hu10D938
date: 2017-04-25 11:38:42
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  with the dark blue contrasted with the gold. Literal strangers stop me in the grocery store or in the elevator and comment on my eyes. The contrast is even more striking in the sun.


human_id: hu548442
date: 2017-04-28 20:52:45
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  eye color tends to change between blue and green (sometimes hazel) with my environment and the color clothes I wear.


human_id: hu217398
date: 2017-05-12 13:12:44
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  blue eyes\nMother: hazel; one iris is larger than other\nFather: light blue\nBrother 1: blue-gray\nBrother 2: brown\n


human_id: hu217398
date: 2017-05-12 13:12:44
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I was born with very dark hair. It became almost bleach blonde very quickly. It darkened with age. Now it is almost brown.


human_id: hu50741B
date: 2017-05-26 18:36:55
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My eyes were much lighter when I was younger.  My mother had brown eyes and my father had blue eyes.


human_id: hu691B95
date: 2017-05-26 20:06:07
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My eyes started out extremely deep blue and as I reached my teen years the color went more hazel. I was raised in the tropics and didn't wear sunglasses until after age 50. My ophthalmologist says I have freckles on the inside of my eyes. My maternal grandmother had glaucoma


human_id: hu691B95
date: 2017-05-26 20:06:07
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  and both my parents were severely near sighted (they thought mom was blind until she got glasses at age 5). I was far sighted after high school. \nHave occasional visual migraines


human_id: hu691B95
date: 2017-05-26 20:06:07
phenotype_category: Basic_Phenotypes:Any final thoughts?
phenotype:
  and got Gray nearly all at once in early age 70s. Mom was deep brown also. I was born white blonde and younger brother was born dark brown.


human_id: hu4F2FC9
date: 2017-05-26 22:44:07
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My eyes are seem to change color with my mood; they tend to be more darker and brown when I am angry


human_id: hu9BBEE6
date: 2017-05-28 12:47:33
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  started with brownish red hair at 3 went almost white blonde. around 5 dirty blonde and 12 yrs brown.Hair still bleaches blonde in strong sunlight


human_id: huF6B050
date: 2017-05-29 19:29:10
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  When I was a child my hair was bleach blonde. In the sun it turns blonde. Without sun it is a dark blonde


human_id: hu99FB1A
date: 2017-05-30 10:21:28
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I remember it being greener when I was younger but that may just be childhood. Maternal grandfather had brown hair and very blue eyes


human_id: hu99FB1A
date: 2017-05-30 10:21:28
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  none of his children do but a few grandchildren have blue eyes. Fairly severe myopia runs in the family


human_id: hu99FB1A
date: 2017-05-30 10:21:28
phenotype_category: Basic_Phenotypes:Any final thoughts?
phenotype:
  Small wrists. I enjoy weight lifting but seem to have a low natural ceiling. Significant body hair on extremities. Hair seems to grow faster than average.


human_id: hu99FB1A
date: 2017-05-30 10:27:31
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  some of the grandchildren do. Mother has severe vision issue not totally corrected with lenses. I have myopia and astigmatism


human_id: hu99FB1A
date: 2017-05-30 10:27:31
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  and eyes so dry I can't wear contacts. Sister doesn't use glasses but has dry eyes and a gland dysfunction.


human_id: hu99FB1A
date: 2017-05-30 10:27:31
phenotype_category: Basic_Phenotypes:Any final thoughts?
phenotype:
  Small wrists and hands. Passionate about weight lifting but traing low ceiling. Short legs relative to torso length. Mothers family are all naturally thin until old age.


human_id: huD58ABC
date: 2017-06-01 17:02:27
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I had a hard time differentiating between the different blue eyes in your photo. #1 looks darker than #2 and #5!


human_id: huF5A4C6
date: 2017-06-06 23:02:25
phenotype_category: Basic_Phenotypes:Any final thoughts?
phenotype:
  My eyes are two different colors. One eye matches my Mothers eye color and the other matched my fathers eye color.


human_id: hu0B51B8
date: 2017-06-21 17:36:33
phenotype_category: Basic_Phenotypes:Any final thoughts?
phenotype:
  I only like men with nice long hair. Bald heads make me cringe but the men who try to talk to me are always bald. Why is that? Can you look in my genes and find that out lol


human_id: hu15E54C
date: 2017-06-24 10:56:44
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  green or yellow. They have gotten lighter and greener with age. My mother and only sibling have very dark brown eyes. My father had light blue eyes.


human_id: hu4EB3D8
date: 2017-06-25 21:57:54
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I was bald at birth\n\nhad golden blonde hair until about 10 years old\n\nhair turned light brown\n\nthen white


human_id: hu4BD9FD
date: 2017-06-27 02:52:37
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My eye color tends to fluctuate wildly from dark browns to light greens (9-20) depending on the day/mood/environment.


human_id: huA2961E
date: 2017-06-29 19:26:59
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I write with my right hand but I throw better with my left - and my left eye and left leg are dominant


human_id: hu7ED49C
date: 2017-07-01 15:18:14
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I was born almost hairless as I understand it.  But had dark brown hair by the time of the age of 2.  Began male pattern as a late teen and am essentially bald except for a 1.5" band of rather thick hair from temple to temple around the lower part of my skull.


human_id: huE778FA
date: 2017-07-02 01:18:00
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  severe male pattern baldness starting in my early 20s (by 23 was completely bald on top).  Started graying in my late 40s


human_id: hu5E55F5
date: 2017-07-02 12:33:44
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  due to medications I have used (eye drops for herpes infections and glaucoma) both eyes have darkened considerably. Only my aunt on my mothers side has also had HSV in one eye. My mother had green eyes


human_id: huF7FFA9
date: 2017-07-04 11:40:06
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  difficult to wear contacts.  Had cataracts removed in both eyes at age 50. Father had macular degeneration


human_id: hu72A81D
date: 2017-07-09 17:17:37
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  one of my sister's has green.  My eyes appear brown unless under direct light and then they could look dark green.  One of my kid's has blue eyes and I understand that both my paternal grandfather (Prussia) and my maternal grandfather (Poland) both had grey eyes.  My father has macular degeneration and glaucoma.  My mother had diabetic glaucoma and cataracts.  All of us wear/wore reading glasses.


human_id: hu72A81D
date: 2017-07-09 17:17:37
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My hair was natural brown until my early thirties and is now gray/brown.  I tend to gray around the sides and ears first.


human_id: hu715C3F
date: 2017-07-10 19:09:11
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  and grandmother have (had) similar eye color.  mine get more coppery and more filled with dark spots when my health is poor.


human_id: hu2C1D94
date: 2017-07-10 23:31:25
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  Born blonde and hair darkened over time. Head hair and beard hair are different colors -- brown with a reddish tint on head


human_id: huC70919
date: 2017-07-15 12:45:19
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My father and sister diagnosed with a lazy eye.  My father's worse so severe that he had it removed and now wears a patch.


human_id: huC70919
date: 2017-07-15 12:45:19
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  When I was a child my hair was very light brown in the summer and medium brown in the winter.  About 45 it turned black as the gray came in.


human_id: huF6EAE7
date: 2017-07-17 23:27:24
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  Hair was very light as a child and then gradually darkened. Still have blonde areas of facial hair and areas with reddish undertones.


human_id: hu83A343
date: 2017-07-19 19:45:43
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My eye doctor said my eyes change color based on my menstrual cycle but she said they were green...my driver license says hazel.\n\nMy eyes were blue when I was young


human_id: huB71785
date: 2017-07-24 17:24:51
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My hair came back curly after chemotherapy as a child.  It has since straightened out again.  In summer I get red-blonde highlights.


human_id: hu9ADF28
date: 2017-07-26 20:38:08
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My eyes have stayed the same my whole life.  I had a grandparent with macular degeneration. I am currently experiencing strabismus.


human_id: hu48C4EB
date: 2017-08-01 21:34:03
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My aunt has magular degeneration.  I was tested on the Farnsworth-Munsell 100 HueColor Vision Test and received 100%.


human_id: hu36A9DD
date: 2017-08-12 11:53:25
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I was born with blond hair that I kept through 4-6 years slowly turning auburn to brown to brown with gray strands


human_id: hu342A08
date: 2017-08-19 15:04:30
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I should have been left-handed but was (kindly) redirected as a young child. I am not fully ambidextrous


human_id: hu342A08
date: 2017-08-19 15:04:30
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  but I am able to do many more things left-handed than a typical "righty" does.  And my regular (right-handed) handwriting is nearly illegible


human_id: hu3DA764
date: 2017-08-20 16:39:40
phenotype_category: Basic_Phenotypes:Right Eye Color - Text Description
phenotype:
  Steel blue with rust colored star burn pattern. Medial 1/4th has faint rim. White flecks on lateral edge


human_id: hu3DA764
date: 2017-08-20 16:39:40
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  when unwashed it looks darker.\n(also%2C technically blonde and blond are one of the few English words with gender distinctions- fiancée/fiancé being the only other I can think of)


human_id: huA6A0FC
date: 2017-08-25 20:38:03
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  Photographic Reference Set (full-size image: https://goo.gl/XQ2Voh) file does not exist at that link.


human_id: hu5A063B
date: 2017-08-26 15:08:43
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My mom has green eyes and my dad has light blue eyes. My eyes look like a perfect combination if you mixed the two colors.  My sister


human_id: hu5A063B
date: 2017-08-26 15:08:43
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  and orange around the pupil - this is different from my mom's eyes which are very uniformly the color of a green olive.


human_id: hu5A063B
date: 2017-08-26 15:08:43
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My hair color is the color that white-blonde hair turns as you get older: looks like the color of a wet sidewalk. Which is grey


human_id: hu5A063B
date: 2017-08-26 15:08:43
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  but it's odd to call it grey because it's not the color grey that people's hair turns when they're old. Dark beige. \n\nWhen I was born I had no hair


human_id: hu5A063B
date: 2017-08-26 15:08:43
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  however my hair was so white and wispy I looked bald until I was 3. Then it slowly darkened to blonde


human_id: hu59BCBE
date: 2017-08-29 12:59:46
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  only two or three strands. my grandmother doesn't have but a few as well. My hair is straight untill it gets long enough to reach my shoulders and then it gets curly. large curls. My father had curly hair.


human_id: hu9EEEEB
date: 2017-09-07 06:54:01
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  it all fell out and came back slowly very thin and strawberry blonde. was lighter as a child. Now much darker


human_id: hu94876C
date: 2017-09-11 13:53:51
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  and brown hair.  Beard and eyebrows still have the red.  The red on my head went to gray about 5 years ago.


human_id: hu94876C
date: 2017-09-11 13:53:51
phenotype_category: Basic_Phenotypes:Any final thoughts?
phenotype:
  I am very interested in all of this stuff.  Hope I get included in anything.  I believe in open source and open source DNA.


human_id: hu7FF48E
date: 2017-10-11 22:24:08
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  just that my eyes change color with cloths and moods but roughly blueish green on outside rusty brownish on inside. I've always been told it is Hazel.  My Maternal Grandmother I guess was Blue


human_id: hu297EDF
date: 2017-10-25 11:12:25
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  Was told I had blue eyes at birth (until ~1 year). \n\nMy father has keratoconus and cataracts. My grandfather had age-related macular degeneration.


human_id: hu297EDF
date: 2017-10-25 11:12:25
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  Was born with blonde hair. Changed at about 1 year. My son has blonde hair (15 months old). My wife indicates she was blonde (now naturally brunette) until about 5 years old.


human_id: hu7F253C
date: 2017-11-06 19:18:52
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  born with white/blonde hair and it stayed that way until teenage years has slowly become reddish/brown and can lighten to a dirty blonde if I get enough sun exposure.


human_id: hu9D979B
date: 2017-11-23 11:18:56
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  Born dark red; turned to auburn; graying started by age 40. Hair texture wavy.\nFather bright red hair


human_id: hu9D979B
date: 2017-11-23 11:18:56
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  the older two (mother with dark brown hair) have bright red (curly) and light brown straight hair.  The younger two (mother with red hair) have light brown straight


human_id: hu4B2CE0
date: 2017-12-07 07:04:32
phenotype_category: Basic_Phenotypes:Any final thoughts?
phenotype:
  I'm surprised that skin tone is not likewise considered here; aren't eye pigments related to melatonin? I've noted that my eyes sometimes grow greener during the summer months when I spend more time outdoors. Would someone with freckles exhibit unusual pigment reactivity to light exposure?


human_id: hu566097
date: 2017-12-09 17:21:03
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My mother's eyesight was perfect up until her death at age 84. She was far-sighted by only 1.50. She did have cataracts removed about 6 months before she died. Her eyes were dark brown. My father's eyes were hazel. more blueish then green. But they also changed color according to his mood. His eyesight was bad. He needed glasses for everything.


human_id: hu566097
date: 2017-12-09 17:21:03
phenotype_category: Basic_Phenotypes:Hair Color - Text Description
phenotype:
  My hair color is a reddish-brown blonde. If I receve a lot of sun my hair changes colors from dark blonde to almost a white blonde.


human_id: hu566097
date: 2017-12-09 17:40:17
phenotype_category: Basic_Phenotypes:Any final thoughts?
phenotype:
  The sunshine will lighten my hair from a reddish-brown-blonde to a white blonde. It also has different textures from thin to thick width.


human_id: hu2C4FD9
date: 2017-12-15 20:53:30
phenotype_category: Basic_Phenotypes:Left Eye Color - Text Description
phenotype:
  Dark blue on the outside and gets lighter blue towards the pupil with a yellow ring around the pupil


human_id: huC8F2AA
date: 2018-01-25 12:04:23
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  All family members have light blue eyes.  I have been told by optometrist that I have very little pigment in my eyes.


human_id: hu6B7AE9
date: 2018-01-28 19:24:58
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  but the amount of hair on my head took a sharp downturn around the onset of my Diabetes & Depression.


human_id: hu64DBF7
date: 2018-01-30 23:13:34
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  one more greenish.\n\nLinks to full-size images not working; descriptions of differences between photos not adequate for making differentiation.


human_id: huF7A4DE
date: 2018-01-30 23:57:58
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  Dark blue ring getting lighter towards the pupil. Symmetrical but my left eye has always been more sensitive to light and wind


human_id: huF7A4DE
date: 2018-01-30 23:57:58
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  while the hair coming from the top of my head is still very light blonde and yellow. It gets lighter when exposed to sunlight for very long!


human_id: hu85F3ED
date: 2018-02-01 22:01:42
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  born blond turned dark reddish brown. lightened in summer sun. turned mixed then grey now. grey started in 40's.


human_id: huB74692
date: 2018-02-03 10:27:07
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  blond as a child; brown as an adult\nwhen hair is wet there is a touch of blond in the white and brown at the roots


human_id: huB74692
date: 2018-02-03 10:27:07
phenotype_category: Basic_Phenotypes:Any final thoughts?
phenotype:
  I was a donor for a few years in the Hartford Farmington area so you may find some surprises\nmy father is colorblind\nmy brother is schizophrenic paranoid tin hat and everything never took meds\nI have Dupuytrenne's- not a problem.


human_id: hu0491FD
date: 2018-02-15 23:08:37
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I was born with dark brown hair that was blond a curly as a child and turned brown-red and wavy as a I got older


human_id: hu5EA636
date: 2018-02-22 13:15:17
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My mother said I was a "toe-head" meaning I was very blonde.  When I was younger my hair would lighten considerably in response to exposure to sunlight


human_id: huCCD063
date: 2018-03-06 09:14:11
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  (Full size image couldn't be found so I did the best comparison from the regular size pictures)\nMy mother has blue/gray eyes and my father had brown eyes. As far as I remember my eyes were always the same color.


human_id: huFBBA79
date: 2018-03-06 21:24:22
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  Started to get white hair in my early 20’s. I’m 37 now and have very prominent white chunky stripes. I’ve never dyed or processed my hair.


human_id: huEAC017
date: 2018-03-13 00:17:17
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  my husband died and I've lost another 50 lbs.  I am working to keep this weight as I'm much healthier and my labs are good though my blood pressure in February


human_id: huEAC017
date: 2018-03-13 00:17:17
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My genetic profile from Ancestry.com is mainly Eastern European as my mother was Czech.  Most of the people on that side of my family have green/brown eyes like mine. Someone once said


human_id: huEAC017
date: 2018-03-13 00:17:17
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  You must be from the Ukraine.  Your eyes look Ukrainian. I'm not from the Ukraine but test out mostly as Eastern European. My eye color is the same as at birth. My father's eyes were blue as are one brother's. My other brother has my eye color


human_id: huEAC017
date: 2018-03-13 00:17:17
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I have a very distinctive hair color at age 68. It's silver. There's no other word for it.  It is NOT gray! It is silky fine and actually too thin now. I noticed the first silver hair at age 21. During my youth


human_id: huEAC017
date: 2018-03-13 00:17:17
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  my hair was plain mouse brown. (No offense%2C mice!) It has never been thick and full.  It is soft and smooth. My father's hair was pure white at his death at age 80. My mother had a beautiful full head of brunette hair but she died at age 35. Her mother's hair was a peppered gray in her old age (80s). My paternal grandmother had soft hair like mine.  They were English


human_id: huEAC017
date: 2018-03-13 00:17:17
phenotype_category: Basic_Phenotypes:Any final thoughts?
phenotype:
  I love participating in any science study that furthers knowledge - because knowledge is power. And who knows?  Perhaps one day


human_id: hu459CF5
date: 2018-03-14 21:54:14
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I recently gained about 30 pounds over about 5 months after falling off a skateboard and breaking my elbow. I have not been running or doing yoga. My average weight prior to injury was in the 160's.\n\n\n\n\n\n


human_id: huFEDD4D
date: 2018-03-22 04:01:40
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My hair in youth up until sometime in elementary school was very platinum blonde. It got darker as I got older and is not a medium golden blonde color.


human_id: huC101E5
date: 2018-04-18 12:51:28
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  cataracts etc. I've always been severely myopic and I've always done ski racing (with helmet) but high impact sport.


human_id: hu50CF0E
date: 2018-05-11 19:50:54
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My father has Usher Syndrome (Type 2). I am a carrier.\nHis father (my paternal grandfather) was colorblind.\nMy mother is near-sighted in one eye and far-sighted in the other.\nSo far


human_id: hu50CF0E
date: 2018-05-11 19:50:54
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  which quickly fell out and grew in golden blonde.\nMy hair started darkening to brown around age 14.\nI started getting grey hairs around age 34.


human_id: hu31FB36
date: 2018-05-21 00:50:38
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I have O type blood but am unsure whether - or +. I am 5’5”; form will not allow me to include height.


human_id: hu31FB36
date: 2018-05-21 00:50:38
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  Father has same eye color with less yellow central heterochromia than me. Mother has brown eyes. Brother has brown eyes with green central heterochromia. Sister has green eyes with brown central heterochromia.


human_id: hu512175
date: 2018-06-15 09:49:25
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  My family has a history of being born with blue eyes and then changes after we go through adolescents.  Most turn a green or aquamarine color.


human_id: hu512175
date: 2018-06-15 09:49:25
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  I was a light dirty dishwasher blonde/blonde growing up but growing older and as I've bleached my hair many many times to make it almost white


human_id: hu512175
date: 2018-06-15 09:49:25
phenotype_category: Basic_Phenotypes:Any final thoughts?
phenotype:
  The photos of the Iris colors are no longer able to be seen any larger than the thumbnails in the survey. The link that you have inserted to take people to larger pictures of the eyes Iris colors doesn't work anymore.


human_id: huB173FD
date: 2018-06-16 05:16:14
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  At birth my eyes were blue according to my sister's diary. My mother's sister has blueish green eyes.


human_id: hu918B47
date: 2018-06-16 22:12:11
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  In the last 5 years of my life I have been told my eyes are blue and gray and I never got those comments before that. Previously it was only blue.


human_id: huA9AFFD
date: 2018-06-21 17:53:39
phenotype_category: Basic_Phenotypes:Comments
phenotype:
  Dad has brown eyes and narrow/closed angle glaucoma. Mom has blue eyes and open angle glaucoma & had cataracts.


