Rare – Page 165 – CheckOrphan

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Morel’s ear

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Turner syndrome

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Monosomy 8q21 q22

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Factor XIII Deficiency

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Congenital disorder of glycosylation type 2B

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Morgellons

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Morgagni-Stewart-Morel syndrome

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Body Integrity Identity Disorder

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Type 2 Idiopathic Macular Telangiectasia

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Mucopolysaccharidosis Type IVA

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