|
DOID:0060675 - catecholaminergic polymorphic ventricular tachycardia 1
Disease Ontology Definition:A catecholaminergic polymorphic ventricular tachycardia that is characterized by autosomal dominant inheritance and has_material_basis_in heterozygous mutation in the RYR2 gene on chromosome 1q43.
Synonyms: CVPT1, arrhythmogenic right ventricular dysplasia 2,
Xenbase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MONDO:0011484 - catecholaminergic polymorphic ventricular tachycardia 1 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee