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Paroxysmal familial ventricular fibrillation

MedGen UID:
Concept ID:
Disease or Syndrome
Synonyms: Idiopathic Ventricular Fibrillation; Idiopathic ventricular fibrillation, not Brugada type; Paroxysmal ventricular fibrillation
Modes of inheritance:
Autosomal dominant inheritance
MedGen UID:
Concept ID:
Intellectual Product
Sources: HPO, OMIM, Orphanet
Autosomal dominant inheritance refers to genetic conditions that occur when a mutation is present in one copy of a given gene (i.e., the person is heterozygous).
not inherited
MedGen UID:
Concept ID:
Intellectual Product
Source: Orphanet
Describes a disorder that is not inherited.
Autosomal dominant inheritance (HPO, OMIM, Orphanet)
not inherited (Orphanet)
SNOMED CT: Paroxysmal familial ventricular fibrillation (233915000)
Related genes: SCN5A, DPP6
OMIM®: 600163
Orphanet: ORPHA228140

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  

Recent clinical studies


McRae JR, Wagner GS, Rogers MC, Canent RV
J Pediatr 1974 Apr;84(4):515-8. PMID: 4834245

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