Skip to Accessibility Menu Skip to Login Skip to Content Skip to Footer

Tell us about your symptom and treatment experience. Take our survey here.

Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency

What is Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency?

A rare form of classic congenital adrenal hyperplasia (CAH) characterized by glucocorticoid deficiency, hyperandrogenism, hypertension and virilization in females.

Other condition names

  • CAH due to 11-beta-hydroxylase deficiency
  • CYP11B1 deficiency

Inheritance type

Autosomal recessive

Age of Onset

  • Infancy
  • Neonatal
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on "https://www.orphadata.com". Data version 1.3.16 / 4.1.7.