steroid inherited metabolic disorder chronic primary adrenal insufficiency hereditary endocrine growth disease adrenogenital syndrome congenital adrenal hyperplasia NANDO:1200397 congenital adrenal gland hyperplasia NANDO:1200396 MONDO:0018479 icd11.foundation:172733763 GARD:0001467 CAH Orphanet:418 NANDO:2100134 UMLS:C0001627 DOID:0050811 adrenogenital disorder MedDRA:10010323 adrenal hyperplasia NANDO:2200370 adrenal hyperplasia, congenital NORD:992 Congenital adrenal hyperplasia (CAH) is an inherited endocrine disorder caused by a steroidogenic enzyme deficiency that is characterized by adrenal insufficiency and variable degrees of hyper or hypo androgyny manifestations, depending of the type and the severity of the disease. MESH:D000312 ICD9:255.2 SCTID:237751000 NCIT:C34360 adrenogenital syndrome MEDGEN:7900