Health Conditions (V) - Genetics Home Reference (V)

Health Conditions - Genetics Home Reference

Health Conditions

Explore the signs and symptoms, genetic cause, and inheritance pattern of various health conditions.

• 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
• 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