All diseases

OMIM ID
232600
OMIM term:
GLYCOGEN STORAGE DISEASE V
Alternative terms:
GSD V; GSD5
MCARDLE DISEASE
MYOPHOSPHORYLASE DEFICIENCY
MUSCLE GLYCOGEN PHOSPHORYLASE DEFICIENCY
PYGM DEFICIENCY
(∗) Location:
11q13.1  
(†) Associated OMIM genes:
PYGM  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/jdde8n7e