Rare – Page 137 – CheckOrphan

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Turner-like syndrome

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Lennox-Gastaut syndrome

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Epimerase deficiency

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Epimetaphyseal dysplasia cataract

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Nystagmus 2- congenital- autosomal dominant

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Tyrosine-oxidase temporary deficiency

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Epilepsy- nocturnal- frontal lobe type

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Epilepsy- partial- familial

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Epilepsy- myoclonic progressive familial

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Chromosome 9- trisomy mosaic

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