hypogonadotropic hypogonadism 7 with or without anosmia

Summary

DOID:0090078 - hypogonadotropic hypogonadism 7 with or without anosmia

Disease Ontology Definition:A hypogonadotropic hypogonadism that has_material_basis_in homozygous or compound heterozygous mutation in the GNRHR gene on chromosome 4q13, sometimes in association with mutation in another gene. No patients with anosmia have been reported.

Synonyms:

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: spry4, il17rd, flrt3, prok2, axl, sema3e, gnrh1, dusp6, fezf1, kiss1r, wdr11, sra1, nsmf, gnrhr, polr3b, [+]

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0007794 - secretion of serous gland

MONDO:0007794 - secretion of serous gland

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)