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Metadata
ID	DOID:0090076
Name	hypogonadotropic hypogonadism 18 with or without anosmia
Definition	A hypogonadotropic hypogonadism that has_material_basis_in heterozygous or homozygous mutation in the IL17RD gene on chromosome 3p14, sometimes in association with mutation in other genes. https://www.ncbi.nlm.nih.gov/pubmed/23643382
Xrefs	ICD10CM:E23.0 MIM:615267
Parent Relationships	is_a autosomal dominant disease is_a hypogonadotropic hypogonadism is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal dominant inheritance has material basis in some autosomal recessive inheritance