Genetic diseases-V
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- 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
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