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Metadata
ID	DOID:0080872
Name	primary ovarian insufficiency 15
Definition	A primary ovarian insufficiency that is characterized by onset of oligomenorrhea in the third decade of life, with small ovaries, reduced number of follicles, and elevated gonadotropic hormones and that has_material_basis_in homozygous mutation in the FANCM gene on chromosome 14q21. https://pubmed.ncbi.nlm.nih.gov/29231814/
Xrefs	MIM:618096
Parent Relationships	is_a primary ovarian insufficiency is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance