Hypogonadotropic hypogonadism 2 with or without anosmia

MONDO:0007844

Any hypogonadotropic hypogonadism in which the cause of the disease is a mutation in the FGFR1 gene.

Also known as: FGFR1 hypogonadotropic hypogonadism, hypogonadotropic hypogonadism 2 with or without anosmia, hypogonadotropic hypogonadism caused by mutation in FGFR1, HH2, KAL2, Kallmann syndrome 2

0 clinical trials for this condition and its sub-types, 0 tagged with Hypogonadotropic hypogonadism 2 with or without anosmia itself.

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Part of

↑ Kallmann syndrome (3)

Including sub-types (0) Tagged with Hypogonadotropic hypogonadism 2 with or without anosmia (0)

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