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Metadata
ID	DOID:0090079
Name	hypogonadotropic hypogonadism 17 with or without anosmia
Definition	A hypogonadotropic hypogonadism that has_material_basis_in heterozygous mutation in the SPRY4 gene on chromosome 5q31, sometimes in association with mutations in other genes. https://www.ncbi.nlm.nih.gov/pubmed/23643382
Xrefs	ICD10CM:E23.0 MIM:615266
Parent Relationships	is_a autosomal dominant disease is_a hypogonadotropic hypogonadism
Subclass Logical Relationships	has material basis in some autosomal dominant inheritance