arrhythmogenic right ventricular dysplasia 10

Summary

DOID:0110081 - arrhythmogenic right ventricular dysplasia 10

Disease Ontology Definition:An arrhythmogenic right ventricular dysplasia that has_material_basis_in heterozygous mutation in the desmoglein-2 gene (DSG2) on chromosome 18q12.

Synonyms: arrhythmogenic right ventricular cardiomyopathy 10, ARVC10, ARVD10, familial arrhythmogenic right ventricular dysplasia 10

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: dsg2

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0012434 - arrhythmogenic right ventricular dysplasia 10

MONDO:0012434 - arrhythmogenic right ventricular dysplasia 10

MIM:

MIM:610193 - ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10; ARVD10

MIM:610193 - ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10; ARVD10

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)