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CRRD ID: 8565847
Species: Homo sapiens
CRRD Object: Variant
Symbol: CV31857
Name: NM_001943.5(DSG2):c.166G>A (p.Val56Met)
Acc ID: DOID:0060674
Term: catecholaminergic polymorphic ventricular tachycardia
Definition: A heart conduction disease characterized by adrenergically induced ventricular tachycardia manifesting as syncope and sudden death during exercise, stress or catecholamine infusion without the presence of structural cardiac abnormalities. (DO)
Definition Source(s): "DO", "DO"
Note: Use of the qualifier "multiple interactions" designates that the annotated interaction is comprised of a complex set of reactions and/or regulatory events, possibly involving additional chemicals and/or gene products.
Object SymbolQualifierEvidenceWithReferenceSourceNotesOriginal Reference(s)
CV31857 IAGP 8554872ClinVarClinVar Annotator: match by term: Stress-induced polymorphic ventricular tachycardia

PMID:17105751, PMID:18678517, PMID:19039334, PMID:20031616, PMID:20031617, PMID:20716751, PMID:20864495, PMID:21606390, PMID:23810883, PMID:23861362, PMID:24033266, PMID:24055113, PMID:25741868, PMID:28492532
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.