Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency
MONDO:0008729Congenital adrenal hyperplasia due to 11 beta-hydroxylase (CYP11B1) deficiency is a rare form of congenital adrenal hyperplasia (CAH) characterized by glucocorticoid deficiency, hyperandrogenism, hypertension and virilization in females.
Also known as: CAH due to 11-beta-hydroxylase deficiency, CYP11B1 deficiency, adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency, 11-Beta-Hydroxylase deficiency, P450C11B1 deficiency, adrenal hyperplasia 4, adrenal hyperplasia IV, adrenal hyperplasia hypertensive form
3 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsBroader categories
Disease
(680)
Metabolic disease
(233)
Inherited lipid metabolism disorder
(189)
Hereditary disease
(176)
Endocrine system disorder
(72)
Inborn errors of metabolism
(45)
Congenital adrenal hyperplasia
(31)
Adrenocortical insufficiency
(26)
Hereditary endocrine growth disease
(24)
Reproductive system disorder
(15)