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Human Disease

primary ovarian insufficiency 17

Term ID
DOID:0080874
Synonyms
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. https://pubmed.ncbi.nlm.nih.gov/30489636/
References
  • MIM:619146
Ontology
Human Disease   ( DOID:0080874 )
Relationships
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