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DO Term : arrhythmogenic right ventricular dysplasia 13 [DOID:0110084] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

An arrhythmogenic right ventricular dysplasia that has_material_basis_in heterozygous mutation in the CTNNA3 gene on chromosome 10q21.

synonyms:
ARVD13,
615616,
OMIM:615616,
familial arrhythmogenic right ventricular dysplasia 13,
ICD10CM:I42.8,
arrhythmogenic right ventricular cardiomyopathy 13,
ARVC13

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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