Rare – Page 563 – CheckOrphan

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Retinpathy anemia CNS anmalies

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Retinhepatendcrinlgic syndrome

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Retinoblastoma

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Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency

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Congenital absence of the sternocleidomastoid muscle

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Cone rod dystrophy amelogenesis imperfecta

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Cone rod dystrophy

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Retinitis pigmentosa-deafness syndrome

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Retinitis pigmentosa mental retardation deafness

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Retinitis pigmentosa

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