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Metadata
ID	DOID:0080870
Name	primary ovarian insufficiency 13
Definition	A primary ovarian insufficiency that has_material_basis_in homozygous mutation in the MSH5 gene on chromosome 6p21. https://pubmed.ncbi.nlm.nih.gov/28175301/
Xrefs	MIM:617442
Parent Relationships	is_a primary ovarian insufficiency is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance