Congenital adrenal hyperplasia

Orpha code: 418OMIM code: 613571

Definicja

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
Klasyfikacja

Clinical group

Synonimy
CAH
Kod ORPHA
418
Kod OMIM
613571
Kod ICD10
E25.0
Kod ICD11
5A71.01

No additional description.

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