Search Ontology:
Human Disease
ovarian dysgenesis 5
- Term ID
- DOID:0080497
- Synonyms
-
- Definition
- A 46 XX gonadal dysgenesis that has_material_basis_in homozygous mutation in the SOHLH1 gene on chromosome 9q34. https://www.omim.org/entry/617690
- References
- Ontology
- Human Disease ( DOID:0080497 )
- is a type of
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