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DOID:0110074 - arrhythmogenic right ventricular dysplasia 5
Disease Ontology Definition:An arrhythmogenic right ventricular dysplasia that has_material_basis_in heterozygous mutation in the TMEM43 gene on chromosome 3p25.
Synonyms: ARVC5, ARVD5, arrhythmogenic right ventricular cardiomyopathy 5, familial arrhythmogenic right ventricular dysplasia 5,
Xenbase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MONDO:0011459 - arrhythmogenic right ventricular dysplasia 5 |
Other Model Organisms: AGR, 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)