ID

45194

Description

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

Keywords

  1. 8/19/22 8/19/22 - Simon Heim
  2. 10/12/22 10/12/22 - Adrian Schulz
Copyright Holder

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

Uploaded on

October 12, 2022

DOI

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License

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
Description

pht003261

Family ID
Description

FAMID

Data type

string

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

SUBJID

Data type

string

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

MOTHER

Data type

string

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

FATHER

Data type

string

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

SEX

Data type

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
Type
Description | Question | Decode (Coded Value)
Data type
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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