Genetic Conditions - V

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Van Bogaert-Bertrand syndrome see Canavan disease

Van der Hoeve syndrome see osteogenesis imperfecta, type I

variegate porphyria

VCFS see 22q11.2 deletion syndrome

Velo-cardio-facial syndrome see 22q11.2 deletion syndrome

Velocardiofacial syndrome see 22q11.2 deletion syndrome

very long-chain acyl-coenzyme A dehydrogenase deficiency

VHL syndrome see von Hippel-Lindau syndrome

Vision Impairment and Blindness see Alström syndrome

VLCAD-C see very long-chain acyl-coenzyme A dehydrogenase deficiency

VLCAD deficiency see very long-chain acyl-coenzyme A dehydrogenase deficiency

VLCAD-H see very long-chain acyl-coenzyme A dehydrogenase deficiency

Von Bogaert-Bertrand disease see Canavan disease

von Hippel-Lindau syndrome

Von Recklenhausen-Applebaum disease see hemochromatosis

von Recklinghausen Disease see neurofibromatosis 1

VP see variegate porphyria

Vrolik disease see osteogenesis imperfecta