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Human Disease

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
Ontology
Human Disease   ( DOID:0090085 )
Relationships
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Genes Involved
Zebrafish Models