A genetically heterogeneous condition, typically inherited in an autosomal recessive fashion, characterized by coenzyme Q10 deficiency.
Comprehensive, easy-to-understand information about this condition
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mitochondrial respiratory chain complex deficiency
MONDO:0000066
giant axonal neuropathy
MONDO:0000128
combined oxidative phosphorylation deficiency
MONDO:0000732
myopathy, lactic acidosis, and sideroblastic anemia
MONDO:0000863
Finnish type amyloidosis
MONDO:0007097
familial amyloid neuropathy
MONDO:0007100