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
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