hypogonadotropic hypogonadism 6 with or without anosmia

Summary

DOID:0090086 - hypogonadotropic hypogonadism 6 with or without anosmia

Disease Ontology Definition:A hypogonadotropic hypogonadism that is characterized by autosomal dominant inheritance and has_material_basis_in heterozygous mutation in the FGF8 gene on chromosome 10q24, sometimes in association with mutation in another gene.

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

: fgf8

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0012988 - hypogonadotropic hypogonadism 6 with or without anosmia

MONDO:0012988 - hypogonadotropic hypogonadism 6 with or without anosmia

MIM:

MIM:612702 - HYPOGONADOTROPIC HYPOGONADISM 6 WITH OR WITHOUT ANOSMIA; HH6

MIM:612702 - HYPOGONADOTROPIC HYPOGONADISM 6 WITH OR WITHOUT ANOSMIA; HH6

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

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

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