Search Ontology:
Human Disease

ovarian dysgenesis 6

Term ID
DOID:0080498
Synonyms
Definition
A 46 XX gonadal dysgenesis that has_material_basis_in homozygous mutation in the NUP107 gene on chromosome 12q15. https://www.omim.org/entry/618078
References
Ontology
Human Disease   ( DOID:0080498 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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