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
D000312Orphanet Code
ORPHA:418congenital adrenal hyperplasia
| MeSH | D000312 |
| Orphanet | ORPHA:418 |
| Treatments | 0 drug(s) |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO