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Summary Literature (0)
DOID:0060676 - catecholaminergic polymorphic ventricular tachycardia 2

Disease Ontology Definition:A catecholaminergic polymorphic ventricular tachycardia that is characterized by autosomal recessive inheritance and has_material_basis_in homozygous or compound heterozygous mutation in the CASQ2 gene on chromosome 1p13.

Synonyms: CVPT2

Xenbase Genes : casq2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012762 - catecholaminergic polymorphic ventricular tachycardia 2


Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): catecholaminergic polymorphic ventricular tachycardia (is_a)