All diseases

OMIM ID
601462
OMIM term:
MYASTHENIC SYNDROME, CONGENITAL, SLOW-CHANNEL; SCCMS
Alternative terms:
MYASTHENIC SYNDROME, CONGENITAL, POSTSYNAPTIC SLOW-CHANNEL
MYASTHENIC SYNDROME, CONGENITAL, TYPE IIa; CMS2A
CMS IIa
(∗) Location:
17p13.1   17p13.2   2q31.1   2q37.1  
(†) Associated OMIM genes:
CHRNA1   CHRNB1   CHRND   CHRNE  
(‡) Associated MGI genes:
Chrne  

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