Hypogonadotropic hypogonadism 6 with or without anosmia

MONDO:0012988

Any hypogonadotropic hypogonadism in which the cause of the disease is a mutation in the FGF8 gene.

Also known as: FGF8 hypogonadotropic hypogonadism, hypogonadotropic hypogonadism 6 with or without anosmia, hypogonadotropic hypogonadism caused by mutation in FGF8, KAL6, HH6, Kallmann syndrome 6

0 clinical trials for this condition and its sub-types, 0 tagged with Hypogonadotropic hypogonadism 6 with or without anosmia itself.

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Part of

↑ Kallmann syndrome (3)

Including sub-types (0) Tagged with Hypogonadotropic hypogonadism 6 with or without anosmia (0)

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