Rare – Page 388 – CheckOrphan

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Crossed polydactyly type 1

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Crisponi syndrome

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Chromosome 10p terminal deletion syndrome

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Crigler Najjar syndrome type 1

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Hyperphosphatemia

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Anti-NMDA Receptor Encephalitis

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Chromosome 10- monosomy 10q

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Glomerulonephritis

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Palmoplantar Keratoderma

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Palmoplantar keratoderma- epidermolytic

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