Summary Literature (0)

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:

In OMIM:

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

In Mondo Disease Ontology:

MONDO:0012988 - hypogonadotropic hypogonadism 6 with or without anosmia

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : fgf8

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