Disease #00295 (VF2 (fibrillation, ventricular, paroxysmal, familial, type 2 (VF-2)), OMIM:612956)

Official abbreviation VF2
Name fibrillation, ventricular, paroxysmal, familial, type 2 (VF-2)
OMIM ID 612956
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene DPP6
Associated tissues -
Disease features -
Remarks -
Date created 2014-01-12 12:37:09 +01:00 (CET)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

1 entry on 1 page. Showing entry 1.
Legend   How to query  

AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Genes screened

Variants in genes

Variants     

Panel size     

Owner     
00004236 - - summary data from a large study; patients from 3 distantly related families and 7/42 independent patients - no Netherlands - - - - - VF2 Idiopathic Ventricular Fibrillation (IVF), sudden death/successfully resuscitated at young age DPP6 DPP6 2 20 Johan den Dunnen
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.