Disease #03040 (POF5 (ovarian failure, premature, type 5 (POF5)), OMIM:611548)
| Official abbreviation |
POF5 |
| Name |
ovarian failure, premature, type 5 (POF5) |
| OMIM ID |
611548 |
| 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 |
NOBOX |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2020-12-01 17:15:41 +01:00 (CET) |
Individuals
|