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linear skin defects with multiple congenital anomalies 3
MONDO:0010494
mitochondrial complex I deficiency, nuclear type 12
MONDO:0026720
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