congenital adrenal hyperplasia

MeSH: D000312ORPHA: 418

Overview

steroid inherited metabolic disorder that is characterized by adrenal insufficiency and variable degrees of hyper- or hypo-androgeny manifestations resulting from steroidogenic enzyme deficiency

Available Treatments (0)

No treatments linked yet

Clinical trials or compassionate use may be available — consult a specialist.

Classification & Codes

MeSH Code

D000312

Orphanet Code

ORPHA:418
congenital adrenal hyperplasia
MeSHD000312
OrphanetORPHA:418
Treatments0 drug(s)
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO