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Summary Literature (0)
DOID:0090083 - hypogonadotropic hypogonadism 2 with or without anosmia


Disease Ontology Definition:A hypogonadotropic hypogonadism that has_material_basis_in heterozygous mutation in the FGFR1 gene on chromosome 8p11, sometimes in association with mutation in other genes.

Synonyms:

Referenced OMIM:
OMIM:147950 - HYPOGONADOTROPIC HYPOGONADISM 2 WITH OR WITHOUT ANOSMIA; HH2

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

Xenbase Genes : fgfr1

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


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Version: 4.14.0
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