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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, MESH:C536512
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 Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
04/30/2024
MGI 6.23 		The Jackson Laboratory