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<span>Genetic Conditions: V</span>
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<p>Explore the signs and symptoms, genetic cause, and inheritance pattern of various health conditions.</p>
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<span class='blue-label'>Other genetic conditions A-Z</span>
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<li><a href="https://medlineplus.gov/genetics/condition-0/" data-alpha="0-9">0-9</a></li>
<li><a href="https://medlineplus.gov/genetics/condition/" data-alpha="A">A</a></li>
<li><a href="https://medlineplus.gov/genetics/condition-b/" data-alpha="B">B</a></li>
<li><a href="https://medlineplus.gov/genetics/condition-c/" data-alpha="C">C</a></li>
<li><a href="https://medlineplus.gov/genetics/condition-d/" data-alpha="D">D</a></li>
<li><a href="https://medlineplus.gov/genetics/condition-e/" data-alpha="E">E</a></li>
<li><a href="https://medlineplus.gov/genetics/condition-f/" data-alpha="F">F</a></li>
<li><a href="https://medlineplus.gov/genetics/condition-g/" data-alpha="G">G</a></li>
<li><a href="https://medlineplus.gov/genetics/condition-h/" data-alpha="H">H</a></li>
<li><a href="https://medlineplus.gov/genetics/condition-i/" data-alpha="I">I</a></li>
<li><a href="https://medlineplus.gov/genetics/condition-j/" data-alpha="J">J</a></li>
<li><a href="https://medlineplus.gov/genetics/condition-k/" data-alpha="K">K</a></li>
<li><a href="https://medlineplus.gov/genetics/condition-l/" data-alpha="L">L</a></li>
<li><a href="https://medlineplus.gov/genetics/condition-m/" data-alpha="M">M</a></li>
<li><a href="https://medlineplus.gov/genetics/condition-n/" data-alpha="N">N</a></li>
<li><a href="https://medlineplus.gov/genetics/condition-o/" data-alpha="O">O</a></li>
<li><a href="https://medlineplus.gov/genetics/condition-p/" data-alpha="P">P</a></li>
<li><a href="https://medlineplus.gov/genetics/condition-q/" data-alpha="Q">Q</a></li>
<li><a href="https://medlineplus.gov/genetics/condition-r/" data-alpha="R">R</a></li>
<li><a href="https://medlineplus.gov/genetics/condition-s/" data-alpha="S">S</a></li>
<li><a href="https://medlineplus.gov/genetics/condition-t/" data-alpha="T">T</a></li>
<li><a href="https://medlineplus.gov/genetics/condition-u/" data-alpha="U">U</a></li>
<li><span class="active">V</span></li>
<li><a href="https://medlineplus.gov/genetics/condition-w/" data-alpha="W">W</a></li>
<li><a href="https://medlineplus.gov/genetics/condition-x/" data-alpha="X">X</a></li>
<li><a href="https://medlineplus.gov/genetics/condition-y/" data-alpha="Y">Y</a></li>
<li><a href="https://medlineplus.gov/genetics/condition-z/" data-alpha="Z">Z</a></li>
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<section>
<ul class="withident breaklist">
<li><a href="https://medlineplus.gov/genetics/condition/vacterl-association/">VACTERL association</a></li>
<li>Vacuolating leukoencephalopathy, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/megalencephalic-leukoencephalopathy-with-subcortical-cysts/">Megalencephalic leukoencephalopathy with subcortical cysts</a></li>
<li>Vacuolating megalencephalic leukoencephalopathy with subcortical cysts, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/megalencephalic-leukoencephalopathy-with-subcortical-cysts/">Megalencephalic leukoencephalopathy with subcortical cysts</a></li>
<li>vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/vexas-syndrome/">VEXAS syndrome</a></li>
<li>Van Bogaert-Scherer-Epstein disease, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/cerebrotendinous-xanthomatosis/">Cerebrotendinous xanthomatosis</a></li>
<li>Van Buchem disease, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/sost-related-sclerosing-bone-dysplasia/">SOST-related sclerosing bone dysplasia</a></li>
<li>Van der Knaap disease, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/megalencephalic-leukoencephalopathy-with-subcortical-cysts/">Megalencephalic leukoencephalopathy with subcortical cysts</a></li>
<li><a href="https://medlineplus.gov/genetics/condition/van-der-woude-syndrome/">Van der Woude syndrome</a></li>
<li>Vanishing white matter disease, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/leukoencephalopathy-with-vanishing-white-matter/">Leukoencephalopathy with vanishing white matter</a></li>
<li>Vanishing white matter leukodystrophy, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/leukoencephalopathy-with-vanishing-white-matter/">Leukoencephalopathy with vanishing white matter</a></li>
<li>Vascular pseudohemophilia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/von-willebrand-disease/">Von Willebrand disease</a></li>
<li>Vasopressin defective diabetes insipidus, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/arginine-vasopressin-deficiency/">Arginine vasopressin deficiency</a></li>
<li>Vasopressin deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/arginine-vasopressin-deficiency/">Arginine vasopressin deficiency</a></li>
<li>Vasopressin-resistant diabetes insipidus, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/arginine-vasopressin-resistance/">Arginine vasopressin resistance</a></li>
<li>VATER association, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/vacterl-association/">VACTERL association</a></li>
<li>VBU, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/vibratory-urticaria/">Vibratory urticaria</a></li>
<li>VCAN-related vitreoretinopathy, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/wagner-syndrome/">Wagner syndrome</a></li>
<li>VCFS, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/22q112-deletion-syndrome/">22q11.2 deletion syndrome</a></li>
<li>VCPDM, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/distal-myopathy-2/">Distal myopathy 2</a></li>
<li>VDDR, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/vitamin-d-dependent-rickets/">Vitamin D-dependent rickets</a></li>
<li>VDRR, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-hypophosphatemic-rickets/">Hereditary hypophosphatemic rickets</a></li>
<li>VDWS, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/van-der-woude-syndrome/">Van der Woude syndrome</a></li>
<li>Velo-cardio-facial syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/22q112-deletion-syndrome/">22q11.2 deletion syndrome</a></li>
<li>Velocardiofacial syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/22q112-deletion-syndrome/">22q11.2 deletion syndrome</a></li>
<li>Veno-occlusive disease and immunodeficiency syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hepatic-veno-occlusive-disease-with-immunodeficiency/">Hepatic veno-occlusive disease with immunodeficiency</a></li>
<li>Venous form of primary pulmonary hypertension, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/pulmonary-veno-occlusive-disease/">Pulmonary veno-occlusive disease</a></li>
<li>Ventricular dysplasia, right, arrhythmogenic, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/arrhythmogenic-right-ventricular-cardiomyopathy/">Arrhythmogenic right ventricular cardiomyopathy</a></li>
<li>Ventricular pre-excitation with arrhythmia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/wolff-parkinson-white-syndrome/">Wolff-Parkinson-White syndrome</a></li>
<li>Ventriculo-radial syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/holt-oram-syndrome/">Holt-Oram syndrome</a></li>
<li>Vertebral cervical fusion syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/klippel-feil-syndrome/">Klippel-Feil syndrome</a></li>
<li>Vertebral fusion with carpal coalition, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/spondylocarpotarsal-synostosis-syndrome/">Spondylocarpotarsal synostosis syndrome</a></li>
<li>Very long-chain acyl coenzyme A dehydrogenase deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/very-long-chain-acyl-coa-dehydrogenase-deficiency/">Very long-chain acyl-CoA dehydrogenase deficiency</a></li>
<li><a href="https://medlineplus.gov/genetics/condition/very-long-chain-acyl-coa-dehydrogenase-deficiency/">Very long-chain acyl-CoA dehydrogenase deficiency</a></li>
<li>Very long-chain acyl-coenzyme A dehydrogenase deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/very-long-chain-acyl-coa-dehydrogenase-deficiency/">Very long-chain acyl-CoA dehydrogenase deficiency</a></li>
<li>VEXAS, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/vexas-syndrome/">VEXAS syndrome</a></li>
<li><a href="https://medlineplus.gov/genetics/condition/vexas-syndrome/">VEXAS syndrome</a></li>
<li>VHL syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/von-hippel-lindau-syndrome/">Von Hippel-Lindau syndrome</a></li>
<li>Vibratory angioedema, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/vibratory-urticaria/">Vibratory urticaria</a></li>
<li><a href="https://medlineplus.gov/genetics/condition/vibratory-urticaria/">Vibratory urticaria</a></li>
<li><a href="https://medlineplus.gov/genetics/condition/vici-syndrome/">Vici syndrome</a></li>
<li>Visceral heterotaxy, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/heterotaxy-syndrome/">Heterotaxy syndrome</a></li>
<li>Vision defect, color, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/color-vision-deficiency/">Color vision deficiency</a></li>
<li>Visser-Cost syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/corticosterone-methyloxidase-deficiency/">Corticosterone methyloxidase deficiency</a></li>
<li>Vitamin B12 metabolic defect with combined deficiency of methylmalonyl-coA mutase and homocysteine:methyltetrahydrofolate methyltransferase, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/methylmalonic-acidemia-with-homocystinuria/">Methylmalonic acidemia with homocystinuria</a></li>
<li>Vitamin B12 metabolic defect with combined deficiency of methylmalonyl-coA mutase and methionine synthase activities, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/methylmalonic-acidemia-with-homocystinuria/">Methylmalonic acidemia with homocystinuria</a></li>
<li>Vitamin B6-dependent seizures, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/pyridoxine-dependent-epilepsy/">Pyridoxine-dependent epilepsy</a></li>
<li>Vitamin D hypersensitivity, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/idiopathic-infantile-hypercalcemia/">Idiopathic infantile hypercalcemia</a></li>
<li><a href="https://medlineplus.gov/genetics/condition/vitamin-d-dependent-rickets/">Vitamin D-dependent rickets</a></li>
<li>Vitamin D-resistant rickets, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-hypophosphatemic-rickets/">Hereditary hypophosphatemic rickets</a></li>
<li>Vitelliform dystrophy, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/vitelliform-macular-dystrophy/">Vitelliform macular dystrophy</a></li>
<li><a href="https://medlineplus.gov/genetics/condition/vitelliform-macular-dystrophy/">Vitelliform macular dystrophy</a></li>
<li><a href="https://medlineplus.gov/genetics/condition/vitiligo/">Vitiligo</a></li>
<li>Vitreoretinochoroidopathy dominant, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/autosomal-dominant-vitreoretinochoroidopathy/">Autosomal dominant vitreoretinochoroidopathy</a></li>
<li>Vitreoretinochoroidopathy with microcornea, glaucoma, and cataract, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/autosomal-dominant-vitreoretinochoroidopathy/">Autosomal dominant vitreoretinochoroidopathy</a></li>
<li>Vitreoretinochoroidopathy, autosomal dominant, with nanophthalmos, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/autosomal-dominant-vitreoretinochoroidopathy/">Autosomal dominant vitreoretinochoroidopathy</a></li>
<li>VLCAD deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/very-long-chain-acyl-coa-dehydrogenase-deficiency/">Very long-chain acyl-CoA dehydrogenase deficiency</a></li>
<li>VLCAD-C, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/very-long-chain-acyl-coa-dehydrogenase-deficiency/">Very long-chain acyl-CoA dehydrogenase deficiency</a></li>
<li>VLCAD-H, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/very-long-chain-acyl-coa-dehydrogenase-deficiency/">Very long-chain acyl-CoA dehydrogenase deficiency</a></li>
<li><a href="https://medlineplus.gov/genetics/condition/vldlr-associated-cerebellar-hypoplasia/">VLDLR-associated cerebellar hypoplasia</a></li>
<li>VLDLR-CH, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/vldlr-associated-cerebellar-hypoplasia/">VLDLR-associated cerebellar hypoplasia</a></li>
<li>VLDLRCH, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/vldlr-associated-cerebellar-hypoplasia/">VLDLR-associated cerebellar hypoplasia</a></li>
<li>VLINCL, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/cln5-disease/">CLN5 disease</a></li>
<li>VMCM, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/multiple-cutaneous-and-mucosal-venous-malformations/">Multiple cutaneous and mucosal venous malformations</a></li>
<li>VMCM1, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/multiple-cutaneous-and-mucosal-venous-malformations/">Multiple cutaneous and mucosal venous malformations</a></li>
<li>Vocal cord and pharyngeal weakness with distal myopathy, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/distal-myopathy-2/">Distal myopathy 2</a></li>
<li>VODI, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hepatic-veno-occlusive-disease-with-immunodeficiency/">Hepatic veno-occlusive disease with immunodeficiency</a></li>
<li><a href="https://medlineplus.gov/genetics/condition/vohwinkel-syndrome/">Vohwinkel syndrome</a></li>
<li>Von Eulenberg&#x27;s disease, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/paramyotonia-congenita/">Paramyotonia congenita</a></li>
<li>Von Gierke disease, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/glycogen-storage-disease-type-i/">Glycogen storage disease type I</a></li>
<li>Von Gierke&#x27;s disease, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/glycogen-storage-disease-type-i/">Glycogen storage disease type I</a></li>
<li>Von Hippel-Lindau disease, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/von-hippel-lindau-syndrome/">Von Hippel-Lindau syndrome</a></li>
<li><a href="https://medlineplus.gov/genetics/condition/von-hippel-lindau-syndrome/">Von Hippel-Lindau syndrome</a></li>
<li>Von Passow syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/horner-syndrome/">Horner syndrome</a></li>
<li>Von Recklenhausen-Applebaum disease, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-hemochromatosis/">Hereditary hemochromatosis</a></li>
<li>Von Recklinghausen disease, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/neurofibromatosis-type-1/">Neurofibromatosis type 1</a></li>
<li><a href="https://medlineplus.gov/genetics/condition/von-willebrand-disease/">Von Willebrand disease</a></li>
<li>Von Willebrand disorder, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/von-willebrand-disease/">Von Willebrand disease</a></li>
<li>Von Willebrand factor receptor deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/bernard-soulier-syndrome/">Bernard-Soulier syndrome</a></li>
<li>Von Willebrand&#x27;s factor deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/von-willebrand-disease/">Von Willebrand disease</a></li>
<li>Von Zumbusch psoriasis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/generalized-pustular-psoriasis/">Generalized pustular psoriasis</a></li>
<li>Vrolik disease, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/osteogenesis-imperfecta/">Osteogenesis imperfecta</a></li>
<li>VWS, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/van-der-woude-syndrome/">Van der Woude syndrome</a></li>
</ul>
</section>
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