visceral heterotaxy

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Echinobase

Summary

Literature (0)

DOID:0050545 - visceral heterotaxy

Disease Ontology Definition:A physical disorder characterized by the abnormal distribution of the major visceral organs within the chest and abdomen.

Synonyms: heterotaxia, situs ambiguus

Echinobase 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

: cfap53

MIM:

MIM:306955 - heterotaxy, visceral, 1, x-linked; htx1
MIM:605376 - heterotaxy, visceral, 2, autosomal; htx2
MIM:613751 - heterotaxy, visceral, 4, autosomal; htx4
MIM:614779 - heterotaxy, visceral, 6, autosomal; htx6

MIM:306955 - heterotaxy, visceral, 1, x-linked; htx1

MIM:605376 - heterotaxy, visceral, 2, autosomal; htx2

MIM:613751 - heterotaxy, visceral, 4, autosomal; htx4

MIM:614779 - heterotaxy, visceral, 6, autosomal; htx6

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

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

Parent(s): physical disorder (is_a)