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DOID:0080172 - thiopurine S-methyltransferase deficiency
Disease Ontology Definition:An inherited metabolic disease that is characterized by significantly reduced activity of an enzyme that helps the body process drugs called thiopurines.
Synonyms: TPMT deficiency, poor metabolism of thiopurines-1,
Echinobase Genes : tpmt
MIM:610460 - thiopurine s-methyltransferase deficiency |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
inherited metabolic disorder (is_a)