hypogonadotropic hypogonadism 18 with or without anosmia

Summary

DOID:0090076 - hypogonadotropic hypogonadism 18 with or without anosmia

Disease Ontology Definition:A hypogonadotropic hypogonadism that has_material_basis_in heterozygous or homozygous mutation in the IL17RD gene on chromosome 3p14, sometimes in association with mutation in other genes.

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

: il17rd

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014103 - hypogonadotropic hypogonadism 18 with or without anosmia

MONDO:0014103 - hypogonadotropic hypogonadism 18 with or without anosmia

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal dominant disease (is_a), autosomal recessive disease (is_a), hypogonadotropic hypogonadism (is_a)