Rare – Page 444 – CheckOrphan

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MHC class 1 or class 2 deficiency

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Mickleson syndrome

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Michels Caskey syndrome

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Primary familial xanthomatosis with involvement and calcification of the adrenal galnds

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Chondrocalcinosis 1

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Micrencephaly olivopontocerebellar hypoplasia

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Micrencephaly corpus callosum agenesis

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Methylmalonyl-Coenzyme A mutase deficiency

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Methylmalonicaciduria with homocystinuria- cbl F

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Meyenburg-Altherr-Uehlinger syndrome

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