Rare – Page 117 – CheckOrphan

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Mitochondrial complex I deficiency

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Mirror polydactyly segmentation and limbs defects

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Mirizzi syndrome

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Minicore myopathy- antenatal onset- with arthrogryposis

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Cataract anterior polar dominant

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Cataract and congenital ichthyosis

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Mitochondrial myopathy with lactic acidosis

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Mitochondrial encephalomyopathy aminoacidopathy

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Mitochondrial diseases- clinically undefined

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Cataract congenital Volkmann type

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