All diseases

OMIM ID
181430
OMIM term:
SCAPULOPERONEAL MYOPATHY, MYH7-RELATED; SPMM
Alternative terms:
SCAPULOPERONEAL MUSCULAR DYSTROPHY; SPMD
SCAPULOPERONEAL SYNDROME, MYOPATHIC TYPE
(∗) Location:
14q11.2  
(†) Associated OMIM genes:
MYH7  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/lb1suyoz