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Human Disease

hypogonadotropic hypogonadism 7 with or without anosmia

Term ID
DOID:0090078
Synonyms
Definition
A hypogonadotropic hypogonadism that has_material_basis_in homozygous or compound heterozygous mutation in the GNRHR gene on chromosome 4q13, sometimes in association with mutation in another gene. No patients with anosmia have been reported. (2)
References
Ontology
Human Disease   ( DOID:0090078 )
Relationships
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Zebrafish Models