ID

45194

Beschreibung

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

Stichworte

  1. 19.08.22 19.08.22 - Simon Heim
  2. 12.10.22 12.10.22 - Adrian Schulz
Rechteinhaber

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

Hochgeladen am

12. Oktober 2022

DOI

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Lizenz

Creative Commons BY 4.0

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

Subject ID, consent group, subject source, and subject source ID 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.

pht003260
Beschreibung

pht003260

Subject ID
Beschreibung

SUBJID

Datentyp

string

Alias
UMLS CUI [1,1]
C2348585
Consent group as determined by DAC
Beschreibung

CONSENT

Datentyp

text

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C1257890
Subject source
Beschreibung

SUBJ_SOURCE

Datentyp

text

Alias
UMLS CUI [1,1]
C0449416
UMLS CUI [1,2]
C0681850
Subject source ID
Beschreibung

SOURCE_SUBJID

Datentyp

text

Alias
UMLS CUI [1,1]
C0681850
UMLS CUI [1,2]
C0449416
UMLS CUI [1,3]
C2348585

Ähnliche Modelle

Subject ID, consent group, subject source, and subject source ID 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
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
pht003260
SUBJID
Item
Subject ID
string
C2348585 (UMLS CUI [1,1])
Item
Consent group as determined by DAC
text
C0021430 (UMLS CUI [1,1])
C1257890 (UMLS CUI [1,2])
Code List
Consent group as determined by DAC
CL Item
Subjects did not participate in the study, did not complete a consent document and are included only for the pedigree structure and/or genotype controls, such as HapMap subjects (0)
CL Item
Disease-Specific (Inflammatory Bowel Disease, IRB) (DS-IBD-IRB) (1)
SUBJ_SOURCE
Item
Subject source
text
C0449416 (UMLS CUI [1,1])
C0681850 (UMLS CUI [1,2])
SOURCE_SUBJID
Item
Subject source ID
text
C0681850 (UMLS CUI [1,1])
C0449416 (UMLS CUI [1,2])
C2348585 (UMLS CUI [1,3])

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