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Metadata
ID DOID:0090085
Name hypogonadotropic hypogonadism 9 with or without anosmia
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.
https://www.ncbi.nlm.nih.gov/pubmed/15362570, https://www.ncbi.nlm.nih.gov/pubmed/17235395
Xrefs

ICD10CM:E23.0

OMIM:614838

Parent Relationships

is_a hypogonadotropic hypogonadism

is_a autosomal dominant disease

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