hypogonadotropic hypogonadism 13 with or without anosmia

Summary

DOID:0090073 - hypogonadotropic hypogonadism 13 with or without anosmia

Disease Ontology Definition:A hypogonadotropic hypogonadism that has_material_basis_in homozygous mutation in the KISS1 gene on chromosome 1q32.

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

: kiss1

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013915 - hypogonadotropic hypogonadism 13 with or without anosmia

MONDO:0013915 - hypogonadotropic hypogonadism 13 with or without anosmia

MIM:

MIM:614842 - HYPOGONADOTROPIC HYPOGONADISM 13 WITH OR WITHOUT ANOSMIA; HH13

MIM:614842 - HYPOGONADOTROPIC HYPOGONADISM 13 WITH OR WITHOUT ANOSMIA; HH13

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)