Disease #02257 (POF1 (ovarian failure, premature, type 1 (POF-1)), OMIM:311360)
Official abbreviation |
POF1 |
Name |
ovarian failure, premature, type 1 (POF-1) |
OMIM ID |
311360 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
X-linked |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
FMR1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
|
|