Thiopurine S-methyltransferase deficiency

MONDO:0012503

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

25 clinical trials for this condition and its sub-types.

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