About   Help   FAQ
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
03/25/2025
MGI 6.24 		The Jackson Laboratory