Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency

MONDO:0008730

A very rare form of congenital adrenal hyperplasia (CAH) characterized by glucocorticoid deficiency, hypergonadotrophic hypogonadism and severe hypokalemic hypertension.

Also known as: 17-alpha-hydroxylase/17,20-lyase deficiency, CAH due to 17-alpha-hydroxylase deficiency, combined 17-hydroxylase/17,20-lyase deficiency, 17,20-lyase deficiency, isolated, 17-Alpha-Hydroxylase deficiency, 17-Alpha-Hydroxylase/17,20-lyase deficiency, combined complete, 17-Alpha-Hydroxylase/17,20-lyase deficiency, combined partial, adrenal hyperplasia 5

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

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