Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
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

Xenbase Genes : fshb

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009239 - hypogonadotropic hypogonadism 24 without anosmia


Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal recessive disease (is_a), hypogonadotropic hypogonadism (is_a)