One of the most common forms of hereditary optic neuropathy characterized by progressive bilateral visual loss during the first decade of life, associated with optic disk pallor, visual field and color vision defects.
Comprehensive, easy-to-understand information about this condition
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mitochondrial respiratory chain complex deficiency
MONDO:0000066
combined oxidative phosphorylation deficiency
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myopathy, lactic acidosis, and sideroblastic anemia
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optic atrophy 3
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Leigh syndrome
MONDO:0009723
mitochondrial non-syndromic sensorineural hearing loss
MONDO:0010779