Search Ontology:
Human Disease
ovarian dysgenesis 7
- Term ID
- DOID:0080499
- Synonyms
-
- Definition
- A 46 XX gonadal dysgenesis that has_material_basis_in homozygous mutation in the MRPS22 gene on chromosome 3q23. https://www.omim.org/entry/618117
- References
- Ontology
- Human Disease ( DOID:0080499 )
- is a type of
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