All diseases

OMIM ID
260005
OMIM term:
5-@OXOPROLINASE DEFICIENCY; OPLAHD
Alternative terms:

(∗) Location:
8q24.3  
(†) Associated OMIM genes:
OPLAH  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/l3s70wzy