hypogonadotropic hypogonadism 5 with or without anosmia

Summary

DOID:0090084 - hypogonadotropic hypogonadism 5 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 CHD7 gene on chromosome 8q12.

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

: chd7

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0012880 - hypogonadotropic hypogonadism 5 with or without anosmia

MONDO:0012880 - hypogonadotropic hypogonadism 5 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)