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Disease Ontology Browser
poor metabolism of thiopurines (DOID:0080172)
Alliance: disease page
Synonyms: thiopurine S-methyltransferase deficiency; TPMT deficiency
Alt IDs: MESH:C536512, OMIM:PS610460
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
12/10/2024
MGI 6.24 		The Jackson Laboratory