Rare – Page 114 – CheckOrphan

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Fructose-1-6-bisphosphatase deficiency

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Cutis laxa- recessive

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Cutis laxa- dominant type

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Cutis laxa corneal clouding mental retardation

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Fructose intolerance

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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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