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| Entry | Name | Description | Category | Pathway | Gene |
|---|---|---|---|---|---|
| H02750 | Glutathionuria | Glutathionuria is a rare disease caused by mutations in GGT1. Most patients presented involvement of the central nervous system in the form of moderate mental retardation, behavioral disturbance, and seizures ... | Inherited metabolic disorder | GGT1 [HSA:2678] [KO:K18592] |
| [ KEGG | DISEASE | DRUG | MEDICUS ] |