All diseases

OMIM ID
222748
OMIM term:
DIHYDROPYRIMIDINASE DEFICIENCY
Alternative terms:
DIHYDROPYRIMIDINURIA
DPYS DEFICIENCY
DPH DEFICIENCY
(∗) Location:
8q22.3  
(†) Associated OMIM genes:
DPYS  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/j64ab9ph