ventricular fibrillation, paroxysmal familial, 2

Preferred Label : ventricular fibrillation, paroxysmal familial, 2;

MeSH note : also known as VF2; associated with mutatins in DPP6;

Origin ID

C567841;

UMLS CUI

C2751829;

Currated CISMeF NLP mapping
- Ventricular fibrillation, paroxysmal familial, 2 [OMIM Phenotype]
MeSH term(s) associated for indexing
- ventricular fibrillation [MeSH Descriptor]
Record concept(s)
- ventricular fibrillation, paroxysmal familial, 2 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Ventricular fibrillation, paroxysmal familial, 2 [OMIM Phenotype]