Hypogonadotropic hypogonadism 5 with or without anosmia

MONDO:0012880

Any hypogonadotropic hypogonadism in which the cause of the disease is a mutation in the CHD7 gene.

Also known as: CHD7 hypogonadotropic hypogonadism, hypogonadotropic hypogonadism 5 with or without anosmia, hypogonadotropic hypogonadism caused by mutation in CHD7, KAL5, HH5, Kallmann syndrome 5

6 clinical trials for this condition and its sub-types.

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