Paroxysmal familial ventricular fibrillation

Synonyms

Idiopathic Ventricular Fibrillation; Idiopathic ventricular fibrillation, non Brugada type; Paroxysmal ventricular fibrillation

Modes of inheritance

Autosomal dominant inheritance

Autosomal dominant inheritance

MedGen UID: 141047, Concept ID: C0443147, Intellectual Product

Source: Orphanet

A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in heterozygotes. In the context of medical genetics, an autosomal dominant disorder is caused when a single copy of the mutant allele is present. Males and females are affected equally, and can both transmit the disorder with a risk of 50% for each child of inheriting the mutant allele.

(Orphanet)
Not genetically inherited

Not genetically inherited

MedGen UID: 988794, Concept ID: CN307044, Finding

Source: Orphanet

clinical entity without genetic inheritance.

(Orphanet)