Details of Disease

General Information of Disease (ID: DISKUUDE)

Disease Name Ventricular fibrillation, paroxysmal familial, 2
Synonyms
VF2; DPP6 ventricular fibrillation (disease); ventricular fibrillation, paroxysmal familial, 2; ventricular fibrillation, paroxysmal familial, type 2; ventricular fibrillation (disease) caused by mutation in DPP6
Definition Any ventricular fibrillation in which the cause of the disease is a mutation in the DPP6 gene.
Disease Hierarchy
DISMT2VZ: Cardiogenetic disease
DISRM7IX: Paroxysmal familial ventricular fibrillation
DISKUUDE: Ventricular fibrillation, paroxysmal familial, 2
Disease Identifiers
MONDO ID
MONDO_0013063
MESH ID
C567841
UMLS CUI
C2751829
OMIM ID
612956
MedGen ID
442823

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)
This Disease Is Related to 1 DOT Molecule(s)
Gene Name DOT ID Evidence Level Mode of Inheritance REF
DPP6 OTWW3H0K Limited Autosomal dominant [1]
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References

1 Classification of Genes: Standardized Clinical Validity Assessment of Gene-Disease Associations Aids Diagnostic Exome Analysis and Reclassifications. Hum Mutat. 2017 May;38(5):600-608. doi: 10.1002/humu.23183. Epub 2017 Feb 13.