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hypogonadotropic hypogonadism 12 with or without anosmia | RareConnect | RareConnect.io

/hypogonadotropic hypogonadism

/hypogonadotropic hypogonadism 12 with or without anosmia

hypogonadotropic hypogonadism 12 with or without anosmia

Rare Disease

MONDO:0013914

Also Known As

eunuchoidism, familial hypogonadotropicfamilial hypogonadotrophic eunuchoidismfamilial idiopathic gonadotrpin deficiencyhypogonadotropic hypogonadism 12 with or without anosmiaFIGDHH12eunuchoidism familial hypogonadotropicfamilial hypogonadotropic eunuchoidismgonadotropin deficiency familial idiopathicgonadotropin deficiency, familial idiopathic

Definition

A hypogonadotropic hypogonadism that has material basis in homozygous mutation in the GNRH1 gene on chromosome 8p21.

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

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Associated Genes

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:227200 ↗OMIM:614841 ↗

GARD

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