ID

45194

Descripción

Principal Investigator: Steven R. Brant, MD, Johns Hopkins University, Baltimore, MD, USA MeSH: Crohn Disease,Colitis, Ulcerative,Inflammatory Bowel Diseases https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000367 The National Institute of Diabetes and Digestive and Kidney Diseases Inflammatory Bowel Disease Genetics Consortium (NIDDK - IBDGC) conducted a genome wide association study (GWAS) using the Human Omni2.5-Quad beadchip from Illumina to identify disease variants associated with familial Crohn's disease. This study includes a subset of individuals from an original cohort of affected subjects and affected/unaffected relatives from a previous linkage scan which showed increased linkage evidence at three novel risk loci. A total of 708 samples were selected based on various criteria for inclusion from the 6 Genetic Research Centers (GRC) in North America that participate in the IBDGC. This project was supported by an ancillary R01 grant from the NIDDK with resources made available through the IBDGC.

Link

dbGaP study = phs000367

Palabras clave

  1. 19/8/22 19/8/22 - Simon Heim
  2. 12/10/22 12/10/22 - Adrian Schulz
Titular de derechos de autor

Steven R. Brant, MD, Johns Hopkins University, Baltimore, MD, USA

Subido en

12 de octubre de 2022

DOI

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Licencia

Creative Commons BY 4.0

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dbGaP phs000367 Genome Wide Association Study in Familial Crohn's Disease

Family ID, subject ID, mother ID, father ID, and sex of participants with or without Crohn's disease and involved in the "NIDDK Inflammatory Bowel Disease Genetics Consortium (IBDGC) Genome Wide Association Study in Familial Crohn's Disease" project.

pht003261
Descripción

pht003261

Family ID
Descripción

FAMID

Tipo de datos

string

Alias
UMLS CUI [1,1]
C0015576
UMLS CUI [1,2]
C0600091
Unique subject ID
Descripción

SUBJID

Tipo de datos

string

Alias
UMLS CUI [1,1]
C2348585
Mother subject ID
Descripción

MOTHER

Tipo de datos

string

Alias
UMLS CUI [1,1]
C2348585
UMLS CUI [1,2]
C0026591
Father subject ID
Descripción

FATHER

Tipo de datos

string

Alias
UMLS CUI [1,1]
C2348585
UMLS CUI [1,2]
C0015671
Gender
Descripción

SEX

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0079399

Similar models

Family ID, subject ID, mother ID, father ID, and sex of participants with or without Crohn's disease and involved in the "NIDDK Inflammatory Bowel Disease Genetics Consortium (IBDGC) Genome Wide Association Study in Familial Crohn's Disease" project.

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
pht003261
FAMID
Item
Family ID
string
C0015576 (UMLS CUI [1,1])
C0600091 (UMLS CUI [1,2])
SUBJID
Item
Unique subject ID
string
C2348585 (UMLS CUI [1,1])
MOTHER
Item
Mother subject ID
string
C2348585 (UMLS CUI [1,1])
C0026591 (UMLS CUI [1,2])
FATHER
Item
Father subject ID
string
C2348585 (UMLS CUI [1,1])
C0015671 (UMLS CUI [1,2])
Item
Gender
text
C0079399 (UMLS CUI [1,1])
Code List
Gender
CL Item
Male (1)
CL Item
Female (2)

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