Rare – Page 189 – CheckOrphan

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Page 189

Aplasia cutis congenita recessive

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Aplasia cutis congenita of limbs recessive

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Osteogenesis imperfecta- type 2A

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Non-24-hour Sleep Wake Disorder

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Narcolepsy

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Chromosome 3- monosomy 3q13

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Chromosome 3- monosomy 3p25

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Pyruvate kinase deficiency- liver type

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Spastic paraplegia 6- autosomal dominant

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Pyruvate carboxylase deficiency

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