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

: cfap53

OMIM:

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: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

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

Parent(s): physical disorder (is_a)