Search Ontology:
Human Disease
primary ovarian insufficiency 12
- Term ID
- DOID:0080869
- Synonyms
-
- Definition
- A primary ovarian insufficiency that has_material_basis_in homozygous mutation in the SYCE1 gene on chromosome 10q26. https://pubmed.ncbi.nlm.nih.gov/25062452/
- References
- Ontology
- Human Disease ( DOID:0080869 )
- is a type of
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