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| Entry | Name | Description | Category | Pathway | Gene |
|---|---|---|---|---|---|
| H02313 | 5-Oxoprolinase deficiency | ... cycle, that represents the primary pathway for glutathione synthesis and degradation. Recently, the OPLAH mutation was reported in two siblings who suffered from 5-oxoprolinuria with a benign clinical ... | Inherited metabolic disorder | OPLAH [HSA:26873] [KO:K01469] |
| [ KEGG | DISEASE | DRUG | MEDICUS ] |