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hypogonadotropic hypogonadism 18 with or without anosmia | RareConnect | RareConnect.io

/Kallmann syndrome

/hypogonadotropic hypogonadism 18 with or without anosmia

hypogonadotropic hypogonadism 18 with or without anosmia

Rare Disease

MONDO:0014103

Also Known As

IL17RD hypogonadotropic hypogonadismhypogonadotropic hypogonadism 18 with or without anosmiahypogonadotropic hypogonadism 18 with or without anosmia, Autosomal recessive, Autosomal dominant, Digenic dominanthypogonadotropic hypogonadism caused by mutation in IL17RDHH18

Definition

Any hypogonadotropic hypogonadism in which the cause of the disease is a mutation in the IL17RD gene.

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:615267 ↗

GARD

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