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Summary Literature (0)
DOID:0110077 - arrhythmogenic right ventricular dysplasia 9

Disease Ontology Definition:An arrhythmogenic right ventricular dysplasia that has_material_basis_in heterozygous mutations in the PKP2 gene on chromosome 12p11.

Synonyms: arrhythmogenic right ventricular cardiomyopathy 9, ARVC9, ARVD9, familial arrhythmogenic right ventricular dysplasia 9

Xenbase Genes : pkp2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012180 - head or neck skin

MIM:
MIM:609040 - ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 9; ARVD9

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)