All diseases

OMIM ID
612540
OMIM term:
MYOPATHY, CONGENITAL, COMPTON-NORTH
Alternative terms:

(∗) Location:
12q12  
(†) Associated OMIM genes:
CNTN1  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/1yk68hcl