poor metabolism of thiopurines

Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Echinobase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

Echinobase

Summary

Literature (0)

DOID:0080172 - poor metabolism of thiopurines

Disease Ontology Definition:An inherited metabolic disease that is characterized by significantly reduced activity of an enzyme that helps the body process drugs called thiopurines.

Synonyms: poor metabolism of thiopurines-1, TPMT deficiency, thiopurine S-methyltransferase deficiency

Echinobase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: tpmt

MIM:

MIM:610460 - thiopurine s-methyltransferase deficiency

MIM:610460 - thiopurine s-methyltransferase deficiency

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal recessive disease (is_a), inherited metabolic disorder (is_a)