Thiopurine S-methyltransferase deficiency

An inherited metabolic disease that is has its basis in the disruption of thiopurine S-methyltransferase activity.

Also known as: TPMT deficiency, inborn error of thiopurine S-methyltransferase activity, inborn thiopurine S-methyltransferase activity disorder, poor metabolism of thiopurines-1, rare inborn error of thiopurine S-methyltransferase activity, thiopurine S-methyltransferase deficiency, 6-mercaptopurine sensitivity, THPM1

1 clinical trial for this condition and its sub-types, 1 tagged with Thiopurine S-methyltransferase deficiency itself.