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Up to: Hereditary endocrine growth disease · Chronic primary adrenal insufficiency · Adrenogenital syndrome · Steroid inherited metabolic disorder

Congenital adrenal hyperplasia

Congenital adrenal hyperplasia (CAH) is an inherited endocrine disorder caused by a steroidogenic enzyme deficiency that is characterized by adrenal insufficiency and variable degrees of hyper or hypo androgyny manifestations, depending of the type and the severity of the disease.

36 trials tagged with this condition →

  • Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency 20 trials Sub-types →
  • Classic congenital adrenal hyperplasia 5 trials
  • Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency 1 trial
  • Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency 1 trial
  • Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency 1 trial
  • Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency 1 trial
  • Congenital lipoid adrenal hyperplasia due to STAR deficency 1 trial Sub-types →
  • Non-classic congenital adrenal hyperplasia 0 trials

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