Rare – Page 370 – CheckOrphan

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Epimetaphyseal skeletal dysplasia

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Nystagmus 3- congenital- autosomal dominant

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Nystagmus 4- congenital- autosomal dominant

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Tricho-dento-osseous syndrome 1

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Trichodermodysplasia dental alterations

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Atypical hemolytic uremic syndrome

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Atypical lipodystrophy

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Trichoodontoonychial dysplasia

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Trichomalacia

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Trichomegaly cataract hereditary spherocytosis

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