All diseases

OMIM ID
607855
OMIM term:
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
Alternative terms:

(∗) Location:
6q22.33  
(†) Associated OMIM genes:
LAMA2  
(‡) Associated MGI genes:
Lama2  

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* quick link - http://q.sanger.ac.uk/s0egelmi