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Summary Literature (0)
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:

In OMIM:
OMIM:146110 - HYPOGONADOTROPIC HYPOGONADISM 7 WITH OR WITHOUT ANOSMIA; HH7

In Mondo Disease Ontology:
MONDO:0007794 - hypogonadotropic hypogonadism 7 with or without anosmia

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

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

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): hypogonadotropic hypogonadism (is_a)