Search Ontology:
Human Disease

ovarian dysgenesis 3

Term ID
DOID:0080495
Synonyms
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 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models