Non-classic congenital adrenal hyperplasia

MONDO:0023601

A milder form of congenital adrenal hyperplasia characterized by decreased activity of an enzyme in the steroidogenic pathway, typically presenting later in life, that does not require life-long cortisol replacement.

Also known as: late-onset congenital adrenal hyperplasia, non-classic congenital adrenal hyperplasia, LOCAH, NCCAH, attenuated congenital adrenal hyperplasia, non classic congenital adrenal hyperplasia

41 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Broader categories

Sort by