ID

45924

Descrizione

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.

collegamento

dbGaP study = phs001053

Keywords

  1. 27/02/24 27/02/24 - Simon Heim
Titolare del copyright

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

Caricato su

27 febbraio 2024

DOI

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Licenza

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
Descrizione

pht007230

Alias
UMLS CUI [1,1]
C3846158 (Other Coding)
LOINC
LA4728-7
Family identifier
Descrizione

FAMILY_ID

Tipo di dati

string

Alias
UMLS CUI [1,1]
C3669174 (Family pedigree identifier)
LOINC
LP173549-9
Subject level identifier
Descrizione

SUBJECT_ID

Tipo di dati

string

Alias
UMLS CUI [1,1]
C2348585 (Clinical Trial Subject Unique Identifier)
Father ID
Descrizione

FATHER

Tipo di dati

string

Alias
UMLS CUI [1,1]
C3669177 (Father identifier)
LOINC
MTHU047348
UMLS CUI [1,2]
C0030761 (genetic pedigree)
Mother ID
Descrizione

MOTHER

Tipo di dati

string

Alias
UMLS CUI [1,1]
C3669352 (Mother identifier)
LOINC
MTHU047347
UMLS CUI [1,2]
C0030761 (genetic pedigree)
Sex
Descrizione

SEX

Tipo di dati

text

Alias
UMLS CUI [1,1]
C0079399 (Gender)
SNOMED
263495000
LOINC
LP61312-2
Superfamily identifier
Descrizione

SUPERFAMILY

Tipo di dati

string

Alias
UMLS CUI [1,1]
C3669174 (Family pedigree identifier)
LOINC
LP173549-9

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
genere
Description | Question | Decode (Coded Value)
Tipo di dati
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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