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Metadata
ID	DOID:0080866
Name	primary ovarian insufficiency 9
Definition	A primary ovarian insufficiency that has_material_basis_in compound heterozygous mutation in the HFM1 gene on chromosome 1p22. https://pubmed.ncbi.nlm.nih.gov/24597873/
Xrefs	MIM:615724
Parent Relationships	is_a primary ovarian insufficiency is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance