Ventricular tachycardia, familial

Preferred Label : Ventricular tachycardia, familial;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Ventricular tachycardia, familial polymorphic;

Inheritance : Autosomal dominant;

Prefixed ID : #192605;

Details

Origin ID

192605;

UMLS CUI

C0340485;

Automatic exact mappings (from CISMeF team)
- Polymorphic Catecholaminergic Ventricular Tachycardia [MeSH Descriptor]
- polymorphic catecholergic ventricular tachycardia [MeSH Supplementary Concept]
Currated CISMeF NLP mapping
- Familial ventricular tachycardia (disorder) [SNOMED CT concept]
- familial polymorphic ventricular tachycardia [MeSH concept]
Genes related to phenotype
- Guanine nucleotide-binding protein, alpha-inhibiting activity polypeptide 2 [OMIM gene]
HPO term(s)
- Abnormality of metabolism/homeostasis [HPO term]
- Autosomal dominant inheritance [HPO term]
- Paroxysmal ventricular tachycardia [HPO term]
- Right bundle branch block [HPO term]
- Sudden cardiac death [HPO term]
Not associated HPO term(s)
- Cardiomyopathy [HPO term]
See also inter- (CISMeF)
- catecholaminergic polymorphic ventricular tachycardia [Disease (Nov.)]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Familial ventricular tachycardia (disorder) [SNOMED CT concept]
- familial polymorphic ventricular tachycardia [MeSH concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients