/autosomal dominant mitochondrial myopathy with exercise intolerance

autosomal dominant mitochondrial myopathy with exercise intolerance

Rare Disease

MONDO:0014532

Also Known As

IMMDmyopathy, isolated mitochondrial, autosomal dominant

Comprehensive, easy-to-understand information about this condition

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Gene data from MyGene.info • Click to view on NCBI Gene

mitochondrial respiratory chain complex deficiency

MONDO:0000066

combined oxidative phosphorylation deficiency

MONDO:0000732

myopathy, lactic acidosis, and sideroblastic anemia

MONDO:0000863

mitochondrial encephalomyopathy

MONDO:0004675

progressive external ophthalmoplegia

MONDO:0005181

optic atrophy 3

MONDO:0008133