Human genes for thiopurine S-methyltransferase deficiency
Thiopurine S-methyltransferase deficiency [DOID:0080172]
An inherited metabolic disease that is characterized by significantly reduced activity of an enzyme that helps the body process drugs called thiopurines.
Synonyms: thiopurine S-methyltransferase deficiency, DOID:0080172, thiopurine Smethyltransferase deficiency, thiopurine S-methyltransferase deficiencies, poor metabolism of thiopurines-1 ...