Congenital adrenal hyperplasia

Orpha code: 418OMIM code: 613571

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.

Disease data
Classification

Clinical group

Synonyms
CAH
ORPHA code
418
OMIM code
613571
ICD10 code
E25.0
ICD11 code
5A71.01

No additional description.

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