primary ovarian insufficiency 17 Disease Ontology Browser

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Disease Ontology Browser

primary ovarian insufficiency 17 (DOID:0080874)
Alliance: disease page
Alt IDs: OMIM:619146
Definition: A primary ovarian insufficiency that is characterized by early cessation of menses after initial menarche, with small ovaries and uterus and that has_material_basis_in homozygous mutation in the XRCC2 gene on chromosome 7q36.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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