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Disease Ontology Browser
catecholaminergic polymorphic ventricular tachycardia 2 (DOID:0060676)
Alliance: disease page
Synonyms: CVPT2
Alt IDs: OMIM:611938, ICD10CM:I47.2
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.

Disease References using Mouse Models (5)

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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last database update
MGI 6.14
The Jackson Laboratory