Any hypogonadotropic hypogonadism in which the cause of the disease is a mutation in the FSHB gene.
Comprehensive, easy-to-understand information about this condition
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hypogonadotropic hypogonadism 23 with or without anosmia
MONDO:0009223
hypogonadotropic hypogonadism 10 with or without anosmia
MONDO:0013912
hypogonadotropic hypogonadism 12 with or without anosmia
MONDO:0013914
hypogonadotropic hypogonadism 13 with or without anosmia
MONDO:0013915
congenital hypogonadotropic hypogonadism
MONDO:0015770
Kallmann syndrome
MONDO:0018800