Disease #00176 (ARVD11 (ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 11), OMIM:610476)

Official abbreviation ARVD11
Name ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 11
OMIM ID 610476
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant, Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene DSG2
Associated tissues -
Disease features -
Remarks -

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