multiple intestinal atresia

Summary

DOID:14671 - multiple intestinal atresia

Disease Ontology Definition:An intestinal disease characterized by the presence of numerous atresic segments in the small and large intestines that has_material_basis_in homozygous or compound heterozygous mutation in the TTC7A gene on chromosome 2p21.

Synonyms: familial intestinal polyatresia syndrome, gastrointestinal defects and immunodeficiency syndrome, GIDID, MEDDRA:10028210, Multiple gastrointestinal atresias, Multiple gastrointestinal atresias (disorder)

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: ttc7a

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0009465 - multiple intestinal atresia

MONDO:0009465 - multiple intestinal atresia

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal recessive disease (is_a), intestinal disease (is_a)