Genetic diseases-V

• VACTERL association
• vacuolating leukoencephalopathy see Megalencephalic leukoencephalopathy with subcortical cysts
• vacuolating megalencephalic leukoencephalopathy with subcortical cysts see Megalencephalic leukoencephalopathy with subcortical cysts
• Van Bogaert-Scherer-Epstein disease see Cerebrotendinous xanthomatosis
• van Buchem disease see SOST-related sclerosing bone dysplasia
• van der Knaap disease see Megalencephalic leukoencephalopathy with subcortical cysts
• Van der Woude syndrome
• vanishing white matter disease see Leukoencephalopathy with vanishing white matter
• vanishing white matter leukodystrophy see Leukoencephalopathy with vanishing white matter
• vascular pseudohemophilia see Von Willebrand disease
• vasopressin defective diabetes insipidus see Neurohypophyseal diabetes insipidus
• vasopressin deficiency see Neurohypophyseal diabetes insipidus
• vasopressin-resistant diabetes insipidus see Nephrogenic diabetes insipidus
• VATER association see VACTERL association
• VBU see Vibratory urticaria
• VCAN-related vitreoretinopathy see Wagner syndrome
• VCFS see 22q11.2 deletion syndrome
• VCPDM see Distal myopathy 2
• VDDR see Vitamin D-dependent rickets
• VDRR see Hereditary hypophosphatemic rickets
• VDWS see Van der Woude syndrome
• velo-cardio-facial syndrome see 22q11.2 deletion syndrome
• velocardiofacial syndrome see 22q11.2 deletion syndrome
• veno-occlusive disease and immunodeficiency syndrome see Hepatic veno-occlusive disease with immunodeficiency
• venous form of primary pulmonary hypertension see Pulmonary veno-occlusive disease
• ventricular dysplasia, right, arrhythmogenic see Arrhythmogenic right ventricular cardiomyopathy
• Ventricular pre-excitation with arrhythmia see Wolff-Parkinson-White syndrome
• ventriculo-radial syndrome see Holt-Oram syndrome
• vertebral cervical fusion syndrome see Klippel-Feil syndrome
• vertebral fusion with carpal coalition see Spondylocarpotarsal synostosis syndrome
• very long-chain acyl coenzyme A dehydrogenase deficiency see Very long-chain acyl-CoA dehydrogenase deficiency
• Very long-chain acyl-CoA dehydrogenase deficiency
• very long-chain acyl-coenzyme A dehydrogenase deficiency see Very long-chain acyl-CoA dehydrogenase deficiency
• VHL syndrome see Von Hippel-Lindau syndrome
• vibratory angioedema see Vibratory urticaria
• Vibratory urticaria
• Vici syndrome
• visceral heterotaxy see Heterotaxy syndrome
• vision defect, color see Color vision deficiency
• Visser-Cost syndrome see Corticosterone methyloxidase deficiency
• vitamin B12 metabolic defect with combined deficiency of methylmalonyl-coA mutase and homocysteine:methyltetrahydrofolate methyltransferase see Methylmalonic acidemia with homocystinuria
• vitamin B12 metabolic defect with combined deficiency of methylmalonyl-coA mutase and methionine synthase activities see Methylmalonic acidemia with homocystinuria
• vitamin B6-dependent seizures see Pyridoxine-dependent epilepsy
• vitamin D hypersensitivity see Idiopathic infantile hypercalcemia
• Vitamin D-dependent rickets
• vitamin D-resistant rickets see Hereditary hypophosphatemic rickets
• vitelliform dystrophy see Vitelliform macular dystrophy
• Vitelliform macular dystrophy
• Vitiligo
• vitreoretinochoroidopathy dominant see Autosomal dominant vitreoretinochoroidopathy
• vitreoretinochoroidopathy with microcornea, glaucoma, and cataract see Autosomal dominant vitreoretinochoroidopathy
• vitreoretinochoroidopathy, autosomal dominant, with nanophthalmos see Autosomal dominant vitreoretinochoroidopathy
• VLCAD deficiency see Very long-chain acyl-CoA dehydrogenase deficiency
• VLCAD-C see Very long-chain acyl-CoA dehydrogenase deficiency
• VLCAD-H see Very long-chain acyl-CoA dehydrogenase deficiency
• VLDLR-associated cerebellar hypoplasia
• VLDLR-CH see VLDLR-associated cerebellar hypoplasia
• VLDLRCH see VLDLR-associated cerebellar hypoplasia
• vLINCL see CLN5 disease
• VMCM see Multiple cutaneous and mucosal venous malformations
• VMCM1 see Multiple cutaneous and mucosal venous malformations
• vocal cord and pharyngeal weakness with distal myopathy see Distal myopathy 2
• VODI see Hepatic veno-occlusive disease with immunodeficiency
• Vohwinkel syndrome
• Von Eulenberg's disease see Paramyotonia congenita
• von Gierke disease see Glycogen storage disease type I
• von Gierke's disease see Glycogen storage disease type I
• von Hippel-Lindau disease see Von Hippel-Lindau syndrome
• Von Hippel-Lindau syndrome
• von Passow syndrome see Horner syndrome
• Von Recklenhausen-Applebaum disease see Hereditary hemochromatosis
• von Recklinghausen Disease see Neurofibromatosis type 1
• Von Willebrand disease
• von Willebrand disorder see Von Willebrand disease
• von Willebrand factor receptor deficiency see Bernard-Soulier syndrome
• von Willebrand's factor deficiency see Von Willebrand disease
• von Zumbusch psoriasis see Generalized pustular psoriasis
• Vrolik disease see Osteogenesis imperfecta
• VTLG see Vitiligo
• VWS see Van der Woude syndrome