Search Ontology:
Human Disease

hypogonadotropic hypogonadism 24 without anosmia

Term ID
DOID:0090088
Synonyms
  • isolated follicle-stimulating hormone deficiency
Definition
A hypogonadotropic hypogonadism that has_material_basis_in homozygous or compound heterozygous mutation in the FSHB gene on chromosome 11p14. (2)
References
  • ICD10CM:E23.6
  • MIM:229070
  • ORDO:52901
Ontology
Human Disease   ( DOID:0090088 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
Citations
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