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:

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

: wdr11

OMIM:

MIM:146110 - hypogonadotropic hypogonadism 7 with or without anosmia; hh7

MIM:146110 - hypogonadotropic hypogonadism 7 with or without anosmia; hh7

Other Model Organisms: AGR, 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)