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DOID:0110084 - arrhythmogenic right ventricular dysplasia 13
Disease Ontology Definition:An arrhythmogenic right ventricular dysplasia that has_material_basis_in heterozygous mutation in the CTNNA3 gene on chromosome 10q21.
Synonyms: ARVC13, ARVD13, arrhythmogenic right ventricular cardiomyopathy 13, familial arrhythmogenic right ventricular dysplasia 13,
Xenbase Genes :
MONDO:0000908 - arrhythmogenic right ventricular dysplasia 13 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
arrhythmogenic right ventricular cardiomyopathy (is_a),
autosomal dominant disease (is_a)