Search Ontology:
Human Disease
primary ovarian insufficiency 5
- Term ID
- DOID:0080862
- Synonyms
-
- Definition
- A primary ovarian insufficiency that has_material_basis_in heterozygous mutation in the NOBOX gene on chromosome 7q35. https://pubmed.ncbi.nlm.nih.gov/17701902/
- References
- Ontology
- Human Disease ( DOID:0080862 )
- is a type of
-
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