hypogonadotropic hypogonadism 9 with or without anosmia

Term ID

DOID:0090085

Synonyms

Definition

A hypogonadotropic hypogonadism that is characterized by autosomal dominant inheritance and has_material_basis_in heterozygous mutation in the NELF gene on chromosome 9q34, sometimes in association with mutation in another gene. (2)

References

• ICD10CM:E23.0
• OMIM:614838

Ontology

Human Disease   ( DOID:0090085 )