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Metadata
ID	DOID:0090092
Name	hypogonadotropic hypogonadism 3 with or without anosmia
Definition	A hypogonadotropic hypogonadism that has_material_basis_in heterozygous mutation in the PROKR2 gene on chromosome 20p12, sometimes in association with mutation in another gene. https://www.ncbi.nlm.nih.gov/pubmed/18559922, https://www.ncbi.nlm.nih.gov/pubmed/17054399
Xrefs	ICD10CM:E23.0 MIM:244200
Parent Relationships	is_a autosomal dominant disease is_a hypogonadotropic hypogonadism
Subclass Logical Relationships	has material basis in some autosomal dominant inheritance