Cytoscape Web
Click node...

Idiopathic ventricular fibrillation, not Brugada type
2 OMIM references -
2 associated genes
20 connected diseases
No signs/symptoms info
Disease Type of connection
Romano-Ward syndrome
Atrial stand still
Autosomal dominant microcephaly
Brugada syndrome
Familial atrial fibrillation
Familial isolated dilated cardiomyopathy
Familial progressive cardiac conduction defect
Familial sick sinus syndrome
Catecholaminergic polymorphic ventricular tachycardia
Congenital analbuminemia
Autosomal dominant limb-girdle muscular dystrophy type 1C
Rippling muscle disease
Familial Alzheimer-like prion disease
Fatal familial insomnia
Gerstmann-Straussler-Scheinker syndrome
Huntington disease-like 1
Inherited Creutzfeldt-Jakob disease
Juvenile myelomonocytic leukemia
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
X-linked non-syndromic intellectual deficit
Synonym(s):
- Familial paroxysmal ventricular fibrillation, not Brugada type
Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease
Classification (ICD10):
- Diseases of the circulatory system -
Epidemiological data:
Class of prevalence: unknown
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal dominant
External references:
2 OMIM references -
No MeSH references
Gene symbol UniProt reference OMIM reference
DPP6 P42658126141
SCN5A Q14524600163
No signs/symptoms info available.