Term Name: poor metabolism of thiopurines
Synonyms: thiopurine S-methyltransferase deficiency, TPMT deficiency
Definition: An inherited metabolic disease that is characterized by significantly reduced activity of an enzyme that helps the body process drugs called thiopurines.
Ontology: Human Disease [DOID:0080172]   ( DOID:0080172 )

Relationships
is a type of: autosomal recessive disease inherited metabolic disorder
has subtype: poor metabolism of thiopurines 1 poor metabolism of thiopurines 2