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
|