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| Entry | Name | Description | Category | Pathway | Gene |
|---|---|---|---|---|---|
| H02545 | Hypertryptophanemia | Hypertryptophanemia (HYPTRP) is a rare inherited metabolic disorder caused by congenital defects of tryptophan metabolism. Tryptophan is a precursor to the neurotransmitters serotonin and melatonin. It ... | Inherited metabolic disorder | (HYPTRP) TDO2 [HSA:6999] [KO:K00453] |
| [ KEGG | DISEASE | DRUG | MEDICUS ] |