Rare – Page 337 – CheckOrphan

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Benign angiitis of the central nervous system

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Bencze syndrome

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Benign autosomal dominant myopathy

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Benign essential blepharospasm

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Benign congenital hypotonia

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Benign familial hematuria

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Benign familial neonatal-infantile seizures

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Benign familial infantile epilepsy

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Chromosome 14- deletion 14q- partial duplication 14p

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Congenital aneurysms of the great vessels

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