Rare – Page 138 – CheckOrphan

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Tyrosine-oxidase temporary deficiency

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Lennox-Gastaut syndrome

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Epimerase deficiency

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Epilepsy- myoclonic progressive familial

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Chromosome 9- trisomy mosaic

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Epilepsy- nocturnal- frontal lobe type

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Epilepsy- partial- familial

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Bright’s Disease

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Chromosome 9- trisomy 9q

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Kleefstra syndrome

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