Catecholaminergic Polymorphic Ventricular Tachycardia Type 1

Preferred Label : Catecholaminergic Polymorphic Ventricular Tachycardia Type 1;

NCIt definition : Polymorphic ventricular tachycardia induced by adrenergic stress. It is inherited in an autosomal dominant pattern and is caused by mutations in the ryanodine receptor 2 (RYR2) gene.;

Details

Origin ID

C123414;

UMLS CUI

C1631597;

Has associated anatomic sites
- Cardiovascular System [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Catecholaminergic polymorphic ventricular tachycardia [ORDO Disease]
- Ventricular tachycardia, catecholaminergic polymorphic, 1, with or without atrial dysfunction and/or dilated cardiomyopathy [OMIM Phenotype]
- catecholaminergic polymorphic ventricular tachycardia [Disease (Nov.)]
- polymorphic catecholergic ventricular tachycardia [MeSH concept]
concept_is_in_subset
- Cellosaurus Disease Terminology [NCIt concept]
- Cellosaurus Terminology [NCIt concept]

Keyword's position in hierarchy(ies) :

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