Search Ontology:
Human Disease
ovarian dysgenesis 1
- Term ID
- DOID:0080493
- Synonyms
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- Definition
- A 46 XX gonadal dysgenesis that has_material_basis_in homozygous or compound heterozygous mutation in the gene encoding follicle-stimulating hormone receptor on chromosome 2p16. https://www.omim.org/entry/233300
- References
- Ontology
- Human Disease ( DOID:0080493 )
- is a type of
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