/mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome

mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome

Rare Disease

MONDO:0044714

Also Known As

mitochondrial myopathy-cerebellar atrophy-pigmentary retinopathy syndromeMMYATmyopathy, mitochondrial, and ataxia

Comprehensive, easy-to-understand information about this condition

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

myopathy, lactic acidosis, and sideroblastic anemia

MONDO:0000863

mitochondrial encephalomyopathy

MONDO:0004675

progressive external ophthalmoplegia

MONDO:0005181

mitochondrial myopathy with a defect in mitochondrial-protein transport

MONDO:0009638

Barth syndrome

MONDO:0010543

mitochondrial myopathy with diabetes

MONDO:0010773