OBO ID: DOID:0080172
Term Name: thiopurine S-methyltransferase deficiency Search Ontology:
Synonyms:
  • poor metabolism of thiopurines-1
  • 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. https://ghr.nlm.nih.gov/condition/thiopurine-s-methyltransferase-deficiency#statistics
References:
Ontology: Human Disease   ( DOID:0080172 )
Relationships
is a type of:
OTHER thiopurine S-methyltransferase deficiency PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
TPMT {Thiopurines, poor metabolism of, 1} 610460
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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