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Metadata
ID	DOID:0080860
Name	primary ovarian insufficiency 3
Definition	A primary ovarian insufficiency that has_material_basis_in heterozygous mutation in the FOXL2 gene on chromosome 3q22. https://pubmed.ncbi.nlm.nih.gov/12149404/
Xrefs	MIM:608996
Parent Relationships	is_a autosomal dominant disease is_a primary ovarian insufficiency
Subclass Logical Relationships	has material basis in some autosomal dominant inheritance