Disease #02517 (PFHB1B (heart block, familial, progressive, type 1B), OMIM:604559)
| Official abbreviation |
PFHB1B |
| Name |
heart block, familial, progressive, type 1B |
| OMIM ID |
604559 |
| 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 |
TRPM4 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|