Disease #00083 (POF15 (PREMATURE OVARIAN FAILURE 15), OMIM:618096)
Official abbreviation |
POF15 |
Name |
PREMATURE OVARIAN FAILURE 15 |
OMIM ID |
618096 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
FANCM |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
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