All diseases

OMIM ID
254300
OMIM term:
MYASTHENIA, LIMB-GIRDLE, FAMILIAL
Alternative terms:
LGM
CONGENITAL MYASTHENIC SYNDROME TYPE Ib; CMS1B
CMS Ib
MYASTHENIC MYOPATHY, FORMERLY
(∗) Location:
1p36.33   4p16.3  
(†) Associated OMIM genes:
AGRN   DOK7  
(‡) Associated MGI genes:
Agrn  

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