Term Name: hypogonadotropic hypogonadism 1 with or without anosmia
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.
Ontology: Human Disease [DOID:0090094]   ( DOID:0090094 )

Relationships
is a type of: hypogonadotropic hypogonadism X-linked recessive disease