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

• ICD10CM:E23.0
• OMIM:146110

Ontology

Human Disease   ( DOID:0090078 )