All diseases

OMIM ID
212138
OMIM term:
CARNITINE-ACYLCARNITINE TRANSLOCASE DEFICIENCY
Alternative terms:

(∗) Location:
3p21.31  
(†) Associated OMIM genes:
SLC25A20  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/j0y7xkro