thiopurine S-methyltransferase deficiency
MONDO:0012503Mondo
Findings
No curated finding names thiopurine S-methyltransferase deficiency yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
An inherited metabolic disease that is has its basis in the disruption of thiopurine S-methyltransferase activity.
Definition from the Mondo Disease Ontology (MONDO:0012503), read 2026-09-29. CC BY 4.0.
Where it sits
- A kind of
Other names
5 names
Resolves to: thiopurine S-methyltransferase deficiency
- Also called
- inborn error of thiopurine S-methyltransferase activityinborn thiopurine S-methyltransferase activity disorderpoor metabolism of thiopurines-1rare inborn error of thiopurine S-methyltransferase activityTPMT deficiency