Celiac disease, susceptibility to, 3

Preferred Label : Celiac disease, susceptibility to, 3;

Symbol : CELIAC3;

CISMeF acronym : CELIAC3;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Gluten-sensitive enteropathy, susceptibility to, 3;

Description : Celiac disease, also known as celiac sprue and gluten-sensitive enteropathy, is a multifactorial disorder of the small intestine that is influenced by both environmental and genetic factors. It is characterized by malabsorption resulting from inflammatory injury to the mucosa of the small intestine after the ingestion of wheat gluten or related rye and barley proteins (summary by Farrell and Kelly, 2002). For additional information and a discussion of genetic heterogeneity of celiac disease, see 212750.;

Prefixed ID : #609755;

Details

Origin ID

609755;

UMLS CUI

C1857845;

Automatic exact mappings (from CISMeF team)
- CTLA4 wt Allele [NCIt concept]
- symbol withdrawn CELIAC3 [HGNC gene]
Broader ORDO disease(s)
- Celiac disease [ORDO Disease]
Genes related to phenotype
- Cytotoxic t lymphocyte-associated 4 [OMIM gene]
ORDO concept(s)
- Celiac disease [ORDO Disease]
Semantic type(s)
- Finding [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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