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| Entry | Name | Description | Category | Pathway | Gene |
|---|---|---|---|---|---|
| H00216 | Congenital adrenal hyperplasia | Congenital adrenal hyperplasia (CAH) is a group of monogenic autosomal recessive disorders due to an enzyme deficiency in steroid biosynthesis. All the adrenal hyperplasia syndromes are examples of mixed ... | Endocrine and metabolic disease |
STAR [HSA:6770] [KO:K16931] HSD3B2 [HSA:3284] [KO:K00070] CYP21A2 [HSA:1589] [KO:K00513] CYP11B1 [HSA:1584] [KO:K00497] CYP17A1 [HSA:1586] [KO:K00512] |
| [ KEGG | DISEASE | DRUG | MEDICUS ] |