Disease #05253 (ATFB18 (fibrillation, atrial, familial, type 18 (ATFB-18)), OMIM:617280)
| Official abbreviation |
ATFB18 |
| Name |
fibrillation, atrial, familial, type 18 (ATFB-18) |
| OMIM ID |
617280 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
MYL4 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2017-03-31 14:15:27 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
|