Rare – Page 115 – CheckOrphan

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Cutis laxa- dominant type

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Cutis laxa corneal clouding mental retardation

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Fryer syndrome

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Fructosuria

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Frydman Cohen Ashenazi syndrome

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Fructose-1-phosphate aldolase deficiency- heredita

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Fructosemia- hereditary

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Frydman Cohen Karmon syndrome

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Infantile onset spinocerebellar ataxia

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Infantile myofibromatosis

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