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Metadata
ID	DOID:0090085
Name	hypogonadotropic hypogonadism 9 with or without anosmia
Definition	A hypogonadotropic hypogonadism that is characterized by autosomal dominant inheritance and has_material_basis_in heterozygous mutation in the NELF gene on chromosome 9q34, sometimes in association with mutation in another gene. https://www.ncbi.nlm.nih.gov/pubmed/15362570, https://www.ncbi.nlm.nih.gov/pubmed/17235395
Xrefs	ICD10CM:E23.0 MIM:614838
Parent Relationships	is_a autosomal dominant disease is_a hypogonadotropic hypogonadism
Subclass Logical Relationships	has material basis in some autosomal dominant inheritance