|
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
Echinobase Genes
:
| 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)