catecholaminergic polymorphic ventricular tachycardia 5 Disease Ontology Browser

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Disease Ontology Browser

catecholaminergic polymorphic ventricular tachycardia 5 (DOID:0060679)
Alliance: disease page
Synonyms: CVPT5
Alt IDs: OMIM:615441, 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 TRDN gene on chromosome 6q22.

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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