Any mitochondrial complex I deficiency in which the cause of the disease is a mutation in the nuclear-encoded genes that encode structural subunits or assembly factors of complex I.
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mitochondrial complex I deficiency, nuclear type 12
MONDO:0026720
mitochondrial complex I deficiency, nuclear type 30
MONDO:0026721
Leber hereditary optic neuropathy, autosomal recessive
MONDO:0030309
mitochondrial complex I deficiency, nuclear type 36
MONDO:0030902
mitochondrial complex I deficiency, nuclear type 37
MONDO:0030997
mitochondrial complex I deficiency, nuclear type 2
MONDO:0032606