Health Conditions
Explore the signs and symptoms, frequency, genetic cause, and inheritance pattern of various conditions, diseases, and syndromes.
- 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
- 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
- Vrolik disease, see osteogenesis imperfecta
- VTLG, see vitiligo
- VWS, see van der Woude syndrome
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