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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:

In OMIM:
OMIM:615266 - HYPOGONADOTROPIC HYPOGONADISM 17 WITH OR WITHOUT ANOSMIA; HH17

In Mondo Disease Ontology:
MONDO:0014102 - hypogonadotropic hypogonadism 17 with or without anosmia

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

Xenbase Genes : spry4

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): hypogonadotropic hypogonadism (is_a)