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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-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