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Disease Ontology Browser
thiopurine S-methyltransferase deficiency (DOID:0080172)
Alliance: disease page
Synonyms: poor metabolism of thiopurines-1; TPMT deficiency
Alt IDs: OMIM:610460
Definition: An inherited metabolic disease that is characterized by significantly reduced activity of an enzyme that helps the body process drugs called thiopurines.

Disease References using Mouse Models (1)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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MGI 6.12
The Jackson Laboratory