Search Ontology:
Human Disease
ovarian dysgenesis 3
- Term ID
- DOID:0080495
- Synonyms
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- Definition
- A 46 XX gonadal dysgenesis that has_material_basis_in homozygous mutation in the PSMC3IP gene on chromosome 17q12-q21. https://www.omim.org/entry/614324
- References
- Ontology
- Human Disease ( DOID:0080495 )
- is a type of
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Genes Involved
Zebrafish Models