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 -
Date created 2023-06-16 09:11:16 +00:00 (UTC)
Date last edited N/A

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