thiopurine S-methyltransferase deficiency
(Q32137157)
inherited metabolic disease that is characterized by significantly reduced activity of an enzyme that helps the body process drugs called thiopurines
inherited metabolic disease that is characterized by significantly reduced activity of an enzyme that helps the body process drugs called thiopurines
Language:
Current Data About
thiopurine S-methyltransferase deficiency
| (P31) |
(Q112193867)
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| (P279) |
(Q1758393)
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| (P2888) |
http://purl.obolibrary.org/obo/DOID_0080172
http://identifiers.org/doid/DOID:0080172
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| (P5008) |
(Q4099686)
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other details
| aliases |
TPMT deficiency poor metabolism of thiopurines-1 Thiopurines, Poor Metabolism of THIOPURINE S-METHYLTRANSFERASE DEFICIENCY |
| description | inherited metabolic disease that is characterized by significantly reduced activity of an enzyme that helps the body process drugs called thiopurines |
External Links
| (P486) |
C536512
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| (P492) |
610460
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| (P665) |
H00964
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| (P699) |
DOID:0080172
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| (P1550) |
3315
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| (P2892) |
C2931223
C0342801 |
| (P5270) |
MONDO_0012503
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| (P7464) |
thiopurine-s-methyltransferase-deficiency
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