Paroxysmal Familial Ventricular Fibrillation-2

Preferred Label : Paroxysmal Familial Ventricular Fibrillation-2;

NCIt synonyms : VF2;

NCIt definition : An autosomal dominant condition caused by mutation(s) in the DPP6 gene, encoding A-type potassium channel modulatory protein DPP6. It is characterized by paroxysms of ventricular fibrillation despite the absence of any structural cardiac anomalies.;

Details

Origin ID

C217089;

Currated CISMeF NLP mapping
- Ventricular fibrillation, paroxysmal familial, 2 [OMIM Phenotype]
- ventricular fibrillation, paroxysmal familial, 2 [MeSH concept]
- ventricular fibrillation, paroxysmal familial, 2 [MeSH Supplementary Concept]
concept_is_in_subset
- Cellosaurus Disease Terminology [NCIt concept]
disease_has_finding
- Rare Lesion [NCIt concept]
disease_mapped_to_gene
- DPP6 Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients