Search Ontology:
Human Disease
primary ovarian insufficiency 13
- Term ID
- DOID:0080870
- Synonyms
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- Definition
- A primary ovarian insufficiency that has_material_basis_in homozygous mutation in the MSH5 gene on chromosome 6p21. https://pubmed.ncbi.nlm.nih.gov/28175301/
- References
- Ontology
- Human Disease ( DOID:0080870 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models