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| Entry | Name | Description | Category | Pathway | Gene |
|---|---|---|---|---|---|
| H00964 | Thiopurine S-methyltransferase deficiency (TPMT deficiency) | Thiopurine S-methyltransferase deficiency (TPMT deficiency) is inherited severe intolerance to thiopurine toxicity, caused by mutation in the TPMT gene. TPMT is part of a cascade of enzymes responsible ... | Inherited metabolic disorder | TPMT [HSA:7172] [KO:K00569] |
| [ KEGG | DISEASE | DRUG | MEDICUS ] |