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Metadata
ID	DOID:0090086
Name	hypogonadotropic hypogonadism 6 with or without anosmia
Definition	A hypogonadotropic hypogonadism that is characterized by autosomal dominant inheritance and has_material_basis_in heterozygous mutation in the FGF8 gene on chromosome 10q24, sometimes in association with mutation in another gene. https://www.ncbi.nlm.nih.gov/pubmed/18596921
Xrefs	ICD10CM:E23.0 MIM:612702
Parent Relationships	is_a autosomal dominant disease is_a hypogonadotropic hypogonadism
Subclass Logical Relationships	has material basis in some autosomal dominant inheritance