FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term hypogonadotropic hypogonadism 1 with or without anosmia ID (Ontology) DOID:0090094 (Human Disease)
Definition A hypogonadotropic hypogonadism that has_material_basis_in mutation in the KAL1 gene on chromosome Xp22.3, sometimes in association with mutation in another gene.
Also Known As "dysplasia olfactogenitalis of de morsier"
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 Genes
 hypogonadotropic hypogonadism 1 with or without anosmia       1
 for disease ribbon | hypogonadotropic hypogonadism 1 with or without anosmia       1
 model of | hypogonadotropic hypogonadism 1 with or without anosmia       1
Spanning Tree (Parents/Children)
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X-linked monogenic disease
 |__X-linked recessive disease_____
hypogonadism                       |
 |__hypogonadotropic hypogonadism__|
                                   hypogonadotropic hypogonadism 1 with or without anosmia  1 rec.
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Is a X-linked recessive disease
hypogonadotropic hypogonadism
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Synonyms
  • "dysplasia olfactogenitalis of de morsier" EXACT
Secondary IDs
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ICD10CM:E23.0
MIM:308700