About   Help   FAQ
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Copyright, and Privacy Statement
Send questions and comments to User Support.
last database update
MGI 6.22
The Jackson Laboratory