All diseases

OMIM ID
608930
OMIM term:
MYASTHENIC SYNDROME, CONGENITAL, FAST-CHANNEL
Alternative terms:

(∗) Location:
17p13.2   2q31.1   2q37.1  
(†) Associated OMIM genes:
CHRNA1   CHRND   CHRNE  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/usvy3cfn