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
- 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
- Published: December 4, 2018
- The resources on this site should not be used as a substitute for professional medical care or advice. Users with questions about a personal health condition should consult with a qualified healthcare professional.
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