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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:

Xenbase Genes : fgf8

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012988 - hypogonadotropic hypogonadism 6 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)