All diseases

OMIM ID
603034
OMIM term:
ENDPLATE ACETYLCHOLINESTERASE DEFICIENCY; EAD
Alternative terms:
ENGEL CONGENITAL MYASTHENIC SYNDROME
MYASTHENIC SYNDROME, CONGENITAL, ENGEL TYPE
CONGENITAL MYASTHENIC SYNDROME TYPE Ic; CMS1C
CMS Ic
(∗) Location:
3p25.1  
(†) Associated OMIM genes:
COLQ  
(‡) Associated MGI genes:

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