Disease #03531 (ATFB12 (fibrillation, atrial, familial, type 12), OMIM:614050)
Official abbreviation |
ATFB12 |
Name |
fibrillation, atrial, familial, type 12 |
OMIM ID |
614050 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
ABCC9 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2023-01-03 13:24:24 +01:00 (CET) |
|