FB2026_03 , released September 17, 2026
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Term hypogonadotropic hypogonadism 8 with or without anosmia ID (Ontology) DOID:0090074 (Human Disease)
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.
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 hypogonadotropic hypogonadism 8 with or without anosmia
 for disease ribbon | hypogonadotropic hypogonadism 8 with or without anosmia
 model of | hypogonadotropic hypogonadism 8 with or without anosmia
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autosomal genetic disease
 |__autosomal recessive disease____
hypogonadism                       |
 |__hypogonadotropic hypogonadism__|
                                   hypogonadotropic hypogonadism 8 with or without anosmia  1 rec.
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Is a autosomal recessive disease
hypogonadotropic hypogonadism
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ICD10CM:E23.0
MIM:614837