All diseases

OMIM ID
255125
OMIM term:
MYOPATHY WITH LACTIC ACIDOSIS, HEREDITARY; HML
Alternative terms:
MYOPATHY WITH EXERCISE INTOLERANCE, SWEDISH TYPE
MYOPATHY WITH DEFICIENCY OF SUCCINATE DEHYDROGENASE AND ACONITASE
MYOGLOBINURIA DUE TO ABNORMAL GLYCOLYSIS
(∗) Location:
12q23.3  
(†) Associated OMIM genes:
ISCU  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/bop66cgu