hypogonadotropic hypogonadism 22 with or without anosmia

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Summary

Literature (0)

DOID:0090081 - hypogonadotropic hypogonadism 22 with or without anosmia

Disease Ontology Definition:A hypogonadotropic hypogonadism that has_material_basis_in homozygous mutation in the FEZF1 gene on chromosome 7q31.

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

: fezf1

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014461 - hypogonadotropic hypogonadism 22 with or without anosmia

MONDO:0014461 - hypogonadotropic hypogonadism 22 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 recessive disease (is_a), hypogonadotropic hypogonadism (is_a)