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hypogonadotropic hypogonadism 1 with or without anosmia | RareConnect | RareConnect.io

/Kallmann syndrome

/hypogonadotropic hypogonadism 1 with or without anosmia

hypogonadotropic hypogonadism 1 with or without anosmia

Rare Disease

MONDO:0010635

Also Known As

ANOS1 hypogonadotropic hypogonadismdysplasia olfactogenitalis of de Morsierhypogonadotropic hypogonadism 1 with or without anosmiahypogonadotropic hypogonadism 1 with or without anosmia (Kallmann syndrome 1), X-linked recessivehypogonadotropic hypogonadism caused by mutation in ANOS1HH1KAL1KMSKallmann syndrome 1Kallmann syndrome, X-linkedKallmann syndrome, type 1, X-linkedanosmic hypogonadismdysplasia Olfactogenitalis of De Morsierhypogonadotropic hypogonadism and anosmia

Definition

The X-linked inherited form of Kallmann syndrome caused by mutation of the KAL1 gene mapped to chromosome Xp22.3.

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:308700 ↗

GARD

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