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DO Term : visceral heterotaxy 13 [DOID:0051027] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A visceral heterotaxy that is characterized by heterotaxy and congenital heart disease and that has_material_basis_in homozygous mutation in the DAND5 gene on chromosome 19p13.

synonyms:
OMIM:621079,
621079

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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