ID

45924

Description

Principal Investigator: Janey L. Wiggs, MD PhD, Massachusetts Eye and Ear, Harvard Medical School, Boston MA USA MeSH: Glaucoma,Exfoliation Syndrome https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs001053 The overall goal of our research is to elucidate the pathogenesis of exfoliation syndrome and the associated glaucoma, making it possible to implement effective screening and prevention strategies and to develop novel therapies. Cases genotyped for this project are from the Nurses Health Study (NHS), the Health Professionals Follow-up Study (HPFS), the Women's Genome Health Study (WGHS), the Massachusetts Eye and Ear Infirmary (MEEI), Mayo Clinic, the University of Iowa, the University of Miami and Duke University Medical Center. Exfoliation syndrome (XFS) is a common condition that is a major risk factor for high-tension open-angle glaucoma, pre-mature cataract formation, and increased risk of complications during cataract surgery. Previous studies suggest that exfoliation syndrome and the related glaucoma (XFG) are genetically complex, and one gene, LOXL1, has been identified as a major genetic risk factor. LOXL1 variants are found in up to 98% of affected patients; however, these same variants are also present in up to 80% of unaffected individuals, indicating that additional genetic and/or environmental factors are necessary for disease development. Samples genotyped for this study are a case set (1,096 samples) and 24 pedigrees (98 samples). Controls for association analyses are selected from the NEIGHBORHOOD study.

Lien

dbGaP study = phs001053

Mots-clés

  1. 27/02/2024 27/02/2024 - Simon Heim
Détendeur de droits

Janey L. Wiggs, MD PhD, Massachusetts Eye and Ear, Harvard Medical School, Boston MA USA

Téléchargé le

27 février 2024

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

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dbGaP phs001053 NEI Exfoliation Genotyping Study

Subject ID, family ID, father ID, mother ID, and superfamily variable of participants with exfoliation syndrome and involved in the "National Eye Institute (NEI) Exfoliation Genotyping Study" project.

pht007230
Description

pht007230

Alias
UMLS CUI [1,1]
C3846158
Family identifier
Description

FAMILY_ID

Type de données

string

Alias
UMLS CUI [1,1]
C3669174
Subject level identifier
Description

SUBJECT_ID

Type de données

string

Alias
UMLS CUI [1,1]
C2348585
Father ID
Description

FATHER

Type de données

string

Alias
UMLS CUI [1,1]
C3669177
UMLS CUI [1,2]
C0030761
Mother ID
Description

MOTHER

Type de données

string

Alias
UMLS CUI [1,1]
C3669352
UMLS CUI [1,2]
C0030761
Sex
Description

SEX

Type de données

text

Alias
UMLS CUI [1,1]
C0079399
Superfamily identifier
Description

SUPERFAMILY

Type de données

string

Alias
UMLS CUI [1,1]
C3669174

Similar models

Subject ID, family ID, father ID, mother ID, and superfamily variable of participants with exfoliation syndrome and involved in the "National Eye Institute (NEI) Exfoliation Genotyping Study" project.

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
pht007230
C3846158 (UMLS CUI [1,1])
FAMILY_ID
Item
Family identifier
string
C3669174 (UMLS CUI [1,1])
SUBJECT_ID
Item
Subject level identifier
string
C2348585 (UMLS CUI [1,1])
FATHER
Item
Father ID
string
C3669177 (UMLS CUI [1,1])
C0030761 (UMLS CUI [1,2])
MOTHER
Item
Mother ID
string
C3669352 (UMLS CUI [1,1])
C0030761 (UMLS CUI [1,2])
Item
Sex
text
C0079399 (UMLS CUI [1,1])
Code List
Sex
CL Item
Male (1)
C0086582 (UMLS CUI [1,1])
CL Item
Female (2)
C0086287 (UMLS CUI [1,1])
SUPERFAMILY
Item
Superfamily identifier
string
C3669174 (UMLS CUI [1,1])

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