All diseases

OMIM ID
605809
OMIM term:
MYASTHENIA, FAMILIAL INFANTILE, 1
Alternative terms:
FIM1
CONGENITAL MYASTHENIC SYNDROME TYPE Ia1; CMS1A1
CMS Ia1
(∗) Location:
17p13  
(†) Associated OMIM genes:
(‡) Associated MGI genes:

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