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catecholaminergic polymorphic ventricular tachycardia 1 (DOID:0060675)
Alliance: disease page
Synonyms: arrhythmogenic right ventricular dysplasia 2; CVPT1
Alt IDs: OMIM:604772, ICD10CM:I42.8, ICD10CM:I47.2
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.

Disease References using Mouse Models (11)
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory