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References OMIM Gene GeneReviews HGMD HGNC
GENATLAS PHENOTYPE
last update : 11/07/2006
Symbol IBD3
Location 6p21.3
HGNC id 13863
Name chronic inflammatory bowel disease, 3
Main clinical features
  • predisposing to Crohn disease and ulcerative colitis . associated with rare VNTR alleles in MUC3, restricted to families with only male affected individuals
  • Genetic determination multigenic
    Function/system disorder digestive tract/gastrointestinal
    Type susceptibility factor