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Metadata
ID	DOID:0090074
Name	hypogonadotropic hypogonadism 8 with or without anosmia
Definition	A hypogonadotropic hypogonadism that has_material_basis_in homozygous or compound heterozygous mutation in the KISS1R gene on chromosome 19p13, sometimes in association with mutation in other genes. https://www.ncbi.nlm.nih.gov/pubmed/14573733, https://www.ncbi.nlm.nih.gov/pubmed/23643382
Xrefs	ICD10CM:E23.0 MIM:614837
Parent Relationships	is_a hypogonadotropic hypogonadism is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance