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Human Disease

hypogonadotropic hypogonadism 1 with or without anosmia

Term ID
DOID:0090094
Synonyms
  • dysplasia olfactogenitalis of de morsier
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. (3)
References
Ontology
Human Disease   ( DOID:0090094 )
Relationships
is a type of
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Genes Involved
Zebrafish Models