Catecholaminergic Polymorphic Ventricular Tachycardia Type 3

Preferred Label : Catecholaminergic Polymorphic Ventricular Tachycardia Type 3;

NCIt synonyms : CPVT3;

NCIt definition : An autosomal recessive subtype of catecholaminergic polymorphic ventricular tachycardia caused by mutation(s) in the TECRL gene, encoding trans-2,3-enoyl-CoA reductase-like.;

NCI Metathesaurus CUI : CL1794158;

Details

Origin ID

C189278;

UMLS CUI

C3151463;

Currated CISMeF NLP mapping
- Ventricular tachycardia, catecholaminergic polymorphic, 3 [OMIM Phenotype]
- catecholaminergic polymorphic ventricular tachycardia 3 [DO Concept]
Has associated anatomic sites
- Cardiovascular System [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Ventricular tachycardia, catecholaminergic polymorphic, 3 [OMIM Phenotype]
concept_is_in_subset
- Cellosaurus Disease Terminology [NCIt concept]
- Cellosaurus Terminology [NCIt concept]

Keyword's position in hierarchy(ies) :

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