Ventricular tachycardia, catecholaminergic polymorphic, 3

Preferred Label : Ventricular tachycardia, catecholaminergic polymorphic, 3;

Symbol : CPVT3;

CISMeF acronym : CPVT3;

Type : Phenotype, molecular basis known;

Description : For a general phenotypic description and a discussion of genetic heterogeneity of CPVT, see 604772.;

Inheritance : Autosomal recessive;

Prefixed ID : #614021;

Détails

Origin ID

614021;

UMLS CUI

C3151463;

Currated CISMeF NLP mapping
- Catecholaminergic Polymorphic Ventricular Tachycardia Type 3 [NCIt concept]
- catecholaminergic polymorphic ventricular tachycardia 3 [DO Concept]
DO Cross reference
- catecholaminergic polymorphic ventricular tachycardia 3 [DO Concept]
Genes related to phenotype
- Trans-2,3-enoyl-coa reductase-like protein [OMIM gene]
HPO term(s)
- Autosomal recessive inheritance [HPO term]
- Bidirectional ventricular tachycardia [HPO term]
- Cardiac arrest [HPO term]
- Childhood onset [HPO term]
- Juvenile onset [HPO term]
- Palpitations [HPO term]
- Paroxysmal ventricular tachycardia [HPO term]
- Polymorphic ventricular tachycardia [HPO term]
- Premature ventricular contraction [HPO term]
- Prolonged QT interval [HPO term]
- Sudden death [HPO term]
- Syncope [HPO term]
- Ventricular fibrillation [HPO term]
- Ventricular tachycardia [HPO term]
- Young adult onset [HPO term]
Not associated HPO term(s)
- Prolonged QTc interval [HPO term]
ORDO concept(s)
- Catecholaminergic polymorphic ventricular tachycardia [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Catecholaminergic Polymorphic Ventricular Tachycardia Type 3 [NCIt concept]
- catecholaminergic polymorphic ventricular tachycardia 3 [DO Concept]

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