Rare – Page 521 – CheckOrphan

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Carnevale syndrome

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Carnitine-acylcarnitine translocase deficiency

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Primary carnitine deficiency

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Carnitine palmitoyltransferase I deficiency

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Carnitine palmitoyltransferase II deficiency

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Multifocal choroiditis

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Multicystic renal dysplasia- bilateral

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Mulliez Roux Loterman syndrome

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Mullerian duct abnormalities galactosemia

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Multicentric osteolysis nephropathy

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