All diseases

OMIM ID
274270
OMIM term:
DIHYDROPYRIMIDINE DEHYDROGENASE DEFICIENCY
Alternative terms:
DPD DEFICIENCY
DPYD DEFICIENCY
THYMINE-URACILURIA, HEREDITARY
PYRIMIDINEMIA, FAMILIAL 5-@FLUOROURACIL TOXICITY, INCLUDED
(∗) Location:
1p21.3  
(†) Associated OMIM genes:
DPYD  
(‡) Associated MGI genes:

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