Congenital adrenal hyperplasia
ORPHA:418· ICD-10 E25.0
Definition
A group of rare inherited endocrine disorders caused by a steroidogenic enzyme deficiency and characterized by adrenal insufficiency and variable degrees of hyper- or hypoandrogenism manifestations, depending on disease type and severity.
- Prevalence
- 1-5 / 10 000
- Inheritance
- Autosomal recessive