hypogonadotropic hypogonadism 17 with or without anosmia

Summary

DOID:0090079 - hypogonadotropic hypogonadism 17 with or without anosmia

Disease Ontology Definition:A hypogonadotropic hypogonadism that has_material_basis_in heterozygous mutation in the SPRY4 gene on chromosome 5q31, sometimes in association with mutations 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

: spry4

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014102 - hypogonadotropic hypogonadism 17 with or without anosmia

MONDO:0014102 - hypogonadotropic hypogonadism 17 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), hypogonadotropic hypogonadism (is_a)