Ventricular fibrillation, paroxysmal familial, 2

Preferred Label : Ventricular fibrillation, paroxysmal familial, 2;

Symbol : VF2;

CISMeF acronym : VF2;

Type : Phenotype, molecular basis known;

Inheritance : Autosomal dominant;

Molecular basis : Susceptibility conferred by mutation in the dipeptidylpeptidase VI gene (DPP6, 126141.0001);

Prefixed ID : #612956;

Details

Origin ID

612956;

UMLS CUI

C2751829;

Automatic exact mappings (from CISMeF team)
- Idiopathic ventricular fibrillation, non Brugada type [ORDO Disease]
Currated CISMeF NLP mapping
- ventricular fibrillation, paroxysmal familial, 2 [MeSH concept]
- ventricular fibrillation, paroxysmal familial, 2 [MeSH Supplementary Concept]
Genes related to phenotype
- Dipeptidyl peptidase VI [OMIM gene]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Premature ventricular contraction [HPO term]
- Sudden cardiac death [HPO term]
- Ventricular fibrillation [HPO term]
ORDO concept(s)
- Idiopathic ventricular fibrillation, non Brugada type [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- ventricular fibrillation, paroxysmal familial, 2 [MeSH Supplementary Concept]
- ventricular fibrillation, paroxysmal familial, 2 [MeSH concept]

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