X-linked adrenal hypoplasia congenita

A X-linked condition characterized by underdevelopment of the adrenal gland and adrenal insufficiency caused by mutation(s) in the NR0B1 gene, resulting in decreased activity of the nuclear receptor protein DAX1, which may be associated with hypogonadotropic hypogonadism.

Also known as: AHC, adrenal hypoplasia congenita, X-linked adrenal hypoplasia congenita, X-linked congenital adrenal hypoplasia, adrenal hypoplasia, congenital, X-linked recessive, AHC with HHG, AHC with isolated gonadotropin deficiency, Addison disease, X-linked

2 clinical trials for this condition and its sub-types, 0 tagged with X-linked adrenal hypoplasia congenita itself.