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Summary Literature (0)
DOID:0090079 - hypogonadotropic hypogonadism 17 with or without anosmia

Disease Ontology Definition:A hypogonadotropic hypogonadism that has_material_basis_in heterozygous mutation in the SPRY4 gene on chromosome 5q31, sometimes in association with mutations in other genes.

Synonyms:

Xenbase Genes : spry4

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014102 - hypogonadotropic hypogonadism 17 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): hypogonadotropic hypogonadism (is_a)