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DOID:0090088 - hypogonadotropic hypogonadism 24 without anosmia
Disease Ontology Definition:A hypogonadotropic hypogonadism that has_material_basis_in homozygous or compound heterozygous mutation in the FSHB gene on chromosome 11p14.
Synonyms: isolated follicle-stimulating hormone deficiency,
Echinobase Genes :
MIM:229070 - follicle-stimulating hormone deficiency, isolated |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
hypogonadotropic hypogonadism (is_a)