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
- vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic syndrome, see VEXAS syndrome
- 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 Arginine vasopressin deficiency
- Vasopressin deficiency, see Arginine vasopressin deficiency
- Vasopressin-resistant diabetes insipidus, see Arginine vasopressin resistance
- 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
- VEXAS, see VEXAS syndrome
- VEXAS syndrome
- 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
- VWS, see Van der Woude syndrome