Prab: CSV import

2025-03-30T00:02:47Z

CSV import

← Older revision		Revision as of 00:02, 30 March 2025
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Prab at 21:01, 18 March 2024

2024-03-18T21:01:10Z

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* '''[https://ghr.nlm.nih.gov/condition/vacterl-association VACTERL association]'''
* '''[[vacuolating leukoencephalopathy]]''' see '''[https://ghr.nlm.nih.gov/condition/megalencephalic-leukoencephalopathy-with-subcortical-cysts Megalencephalic leukoencephalopathy with subcortical cysts]'''
* '''[[vacuolating megalencephalic leukoencephalopathy with subcortical cysts]]''' see '''[https://ghr.nlm.nih.gov/condition/megalencephalic-leukoencephalopathy-with-subcortical-cysts Megalencephalic leukoencephalopathy with subcortical cysts]'''
* '''[[Van Bogaert-Scherer-Epstein disease]]''' see '''[https://ghr.nlm.nih.gov/condition/cerebrotendinous-xanthomatosis Cerebrotendinous xanthomatosis]'''
* '''[[van Buchem disease]]''' see '''[https://ghr.nlm.nih.gov/condition/sost-related-sclerosing-bone-dysplasia SOST-related sclerosing bone dysplasia]'''
* '''[[van der Knaap disease]]''' see '''[https://ghr.nlm.nih.gov/condition/megalencephalic-leukoencephalopathy-with-subcortical-cysts Megalencephalic leukoencephalopathy with subcortical cysts]'''
* '''[https://ghr.nlm.nih.gov/condition/van-der-woude-syndrome Van der Woude syndrome]'''
* '''[[vanishing white matter disease]]''' see '''[https://ghr.nlm.nih.gov/condition/leukoencephalopathy-with-vanishing-white-matter Leukoencephalopathy with vanishing white matter]'''
* '''[[vanishing white matter leukodystrophy]]''' see '''[https://ghr.nlm.nih.gov/condition/leukoencephalopathy-with-vanishing-white-matter Leukoencephalopathy with vanishing white matter]'''
* '''[[vascular pseudohemophilia]]''' see '''[https://ghr.nlm.nih.gov/condition/von-willebrand-disease Von Willebrand disease]'''
* '''[[vasopressin defective diabetes insipidus]]''' see '''[https://ghr.nlm.nih.gov/condition/neurohypophyseal-diabetes-insipidus Neurohypophyseal diabetes insipidus]'''
* '''[[vasopressin deficiency]]''' see '''[https://ghr.nlm.nih.gov/condition/neurohypophyseal-diabetes-insipidus Neurohypophyseal diabetes insipidus]'''
* '''[[vasopressin-resistant diabetes insipidus]]''' see '''[https://ghr.nlm.nih.gov/condition/nephrogenic-diabetes-insipidus Nephrogenic diabetes insipidus]'''
* '''[[VATER association]]''' see '''[https://ghr.nlm.nih.gov/condition/vacterl-association VACTERL association]'''
* '''[[VBU]]''' see '''[https://ghr.nlm.nih.gov/condition/vibratory-urticaria Vibratory urticaria]'''
* '''[[VCAN-related vitreoretinopathy]]''' see '''[https://ghr.nlm.nih.gov/condition/wagner-syndrome Wagner syndrome]'''
* '''[[VCFS]]''' see '''[https://ghr.nlm.nih.gov/condition/22q112-deletion-syndrome 22q11.2 deletion syndrome]'''
* '''[[VCPDM]]''' see '''[https://ghr.nlm.nih.gov/condition/distal-myopathy-2 Distal myopathy 2]'''
* '''[[VDDR]]''' see '''[https://ghr.nlm.nih.gov/condition/vitamin-d-dependent-rickets Vitamin D-dependent rickets]'''
* '''[[VDRR]]''' see '''[https://ghr.nlm.nih.gov/condition/hereditary-hypophosphatemic-rickets Hereditary hypophosphatemic rickets]'''
* '''[[VDWS]]''' see '''[https://ghr.nlm.nih.gov/condition/van-der-woude-syndrome Van der Woude syndrome]'''
* '''[[velo-cardio-facial syndrome]]''' see '''[https://ghr.nlm.nih.gov/condition/22q112-deletion-syndrome 22q11.2 deletion syndrome]'''
* '''[[velocardiofacial syndrome]]''' see '''[https://ghr.nlm.nih.gov/condition/22q112-deletion-syndrome 22q11.2 deletion syndrome]'''
* '''[[veno-occlusive disease and immunodeficiency syndrome]]''' see '''[https://ghr.nlm.nih.gov/condition/hepatic-veno-occlusive-disease-with-immunodeficiency Hepatic veno-occlusive disease with immunodeficiency]'''
* '''[[venous form of primary pulmonary hypertension]]''' see '''[https://ghr.nlm.nih.gov/condition/pulmonary-veno-occlusive-disease Pulmonary veno-occlusive disease]'''
* '''[[ventricular dysplasia, right, arrhythmogenic]]''' see '''[https://ghr.nlm.nih.gov/condition/arrhythmogenic-right-ventricular-cardiomyopathy Arrhythmogenic right ventricular cardiomyopathy]'''
* '''[[Ventricular pre-excitation with arrhythmia]]''' see '''[https://ghr.nlm.nih.gov/condition/wolff-parkinson-white-syndrome Wolff-Parkinson-White syndrome]'''
* '''[[ventriculo-radial syndrome]]''' see '''[https://ghr.nlm.nih.gov/condition/holt-oram-syndrome Holt-Oram syndrome]'''
* '''[[vertebral cervical fusion syndrome]]''' see '''[https://ghr.nlm.nih.gov/condition/klippel-feil-syndrome Klippel-Feil syndrome]'''
* '''[[vertebral fusion with carpal coalition]]''' see '''[https://ghr.nlm.nih.gov/condition/spondylocarpotarsal-synostosis-syndrome Spondylocarpotarsal synostosis syndrome]'''
* '''[[very long-chain acyl coenzyme A dehydrogenase deficiency]]''' see '''[https://ghr.nlm.nih.gov/condition/very-long-chain-acyl-coa-dehydrogenase-deficiency Very long-chain acyl-CoA dehydrogenase deficiency]'''
* '''[https://ghr.nlm.nih.gov/condition/very-long-chain-acyl-coa-dehydrogenase-deficiency Very long-chain acyl-CoA dehydrogenase deficiency]'''
* '''[[very long-chain acyl-coenzyme A dehydrogenase deficiency]]''' see '''[https://ghr.nlm.nih.gov/condition/very-long-chain-acyl-coa-dehydrogenase-deficiency Very long-chain acyl-CoA dehydrogenase deficiency]'''
* '''[[VHL syndrome]]''' see '''[https://ghr.nlm.nih.gov/condition/von-hippel-lindau-syndrome Von Hippel-Lindau syndrome]'''
* '''[[vibratory angioedema]]''' see '''[https://ghr.nlm.nih.gov/condition/vibratory-urticaria Vibratory urticaria]'''
* '''[https://ghr.nlm.nih.gov/condition/vibratory-urticaria Vibratory urticaria]'''
* '''[https://ghr.nlm.nih.gov/condition/vici-syndrome Vici syndrome]'''
* '''[[visceral heterotaxy]]''' see '''[https://ghr.nlm.nih.gov/condition/heterotaxy-syndrome Heterotaxy syndrome]'''
* '''[[vision defect, color]]''' see '''[https://ghr.nlm.nih.gov/condition/color-vision-deficiency Color vision deficiency]'''
* '''[[Visser-Cost syndrome]]''' see '''[https://ghr.nlm.nih.gov/condition/corticosterone-methyloxidase-deficiency Corticosterone methyloxidase deficiency]'''
* '''[[vitamin B12 metabolic defect with combined deficiency of methylmalonyl-coA mutase and homocysteine:methyltetrahydrofolate methyltransferase]]''' see '''[https://ghr.nlm.nih.gov/condition/methylmalonic-acidemia-with-homocystinuria Methylmalonic acidemia with homocystinuria]'''
* '''[[vitamin B12 metabolic defect with combined deficiency of methylmalonyl-coA mutase and methionine synthase activities]]''' see '''[https://ghr.nlm.nih.gov/condition/methylmalonic-acidemia-with-homocystinuria Methylmalonic acidemia with homocystinuria]'''
* '''[[vitamin B6-dependent seizures]]''' see '''[https://ghr.nlm.nih.gov/condition/pyridoxine-dependent-epilepsy Pyridoxine-dependent epilepsy]'''
* '''[[vitamin D hypersensitivity]]''' see '''[https://ghr.nlm.nih.gov/condition/idiopathic-infantile-hypercalcemia Idiopathic infantile hypercalcemia]'''
* '''[https://ghr.nlm.nih.gov/condition/vitamin-d-dependent-rickets Vitamin D-dependent rickets]'''
* '''[[vitamin D-resistant rickets]]''' see '''[https://ghr.nlm.nih.gov/condition/hereditary-hypophosphatemic-rickets Hereditary hypophosphatemic rickets]'''
* '''[[vitelliform dystrophy]]''' see '''[https://ghr.nlm.nih.gov/condition/vitelliform-macular-dystrophy Vitelliform macular dystrophy]'''
* '''[https://ghr.nlm.nih.gov/condition/vitelliform-macular-dystrophy Vitelliform macular dystrophy]'''
* '''[https://ghr.nlm.nih.gov/condition/vitiligo Vitiligo]'''
* '''[[vitreoretinochoroidopathy dominant]]''' see '''[https://ghr.nlm.nih.gov/condition/autosomal-dominant-vitreoretinochoroidopathy Autosomal dominant vitreoretinochoroidopathy]'''
* '''[[vitreoretinochoroidopathy with microcornea, glaucoma, and cataract]]''' see '''[https://ghr.nlm.nih.gov/condition/autosomal-dominant-vitreoretinochoroidopathy Autosomal dominant vitreoretinochoroidopathy]'''
* '''[[vitreoretinochoroidopathy, autosomal dominant, with nanophthalmos]]''' see '''[https://ghr.nlm.nih.gov/condition/autosomal-dominant-vitreoretinochoroidopathy Autosomal dominant vitreoretinochoroidopathy]'''
* '''[[VLCAD deficiency]]''' see '''[https://ghr.nlm.nih.gov/condition/very-long-chain-acyl-coa-dehydrogenase-deficiency Very long-chain acyl-CoA dehydrogenase deficiency]'''
* '''[[VLCAD-C]]''' see '''[https://ghr.nlm.nih.gov/condition/very-long-chain-acyl-coa-dehydrogenase-deficiency Very long-chain acyl-CoA dehydrogenase deficiency]'''
* '''[[VLCAD-H]]''' see '''[https://ghr.nlm.nih.gov/condition/very-long-chain-acyl-coa-dehydrogenase-deficiency Very long-chain acyl-CoA dehydrogenase deficiency]'''
* '''[https://ghr.nlm.nih.gov/condition/vldlr-associated-cerebellar-hypoplasia VLDLR-associated cerebellar hypoplasia]'''
* '''[[VLDLR-CH]]''' see '''[https://ghr.nlm.nih.gov/condition/vldlr-associated-cerebellar-hypoplasia VLDLR-associated cerebellar hypoplasia]'''
* '''[[VLDLRCH]]''' see '''[https://ghr.nlm.nih.gov/condition/vldlr-associated-cerebellar-hypoplasia VLDLR-associated cerebellar hypoplasia]'''
* '''[[vLINCL]]''' see '''[https://ghr.nlm.nih.gov/condition/cln5-disease CLN5 disease]'''
* '''[[VMCM]]''' see '''[https://ghr.nlm.nih.gov/condition/multiple-cutaneous-and-mucosal-venous-malformations Multiple cutaneous and mucosal venous malformations]'''
* '''[[VMCM1]]''' see '''[https://ghr.nlm.nih.gov/condition/multiple-cutaneous-and-mucosal-venous-malformations Multiple cutaneous and mucosal venous malformations]'''
* '''[[vocal cord and pharyngeal weakness with distal myopathy]]''' see '''[https://ghr.nlm.nih.gov/condition/distal-myopathy-2 Distal myopathy 2]'''
* '''[[VODI]]''' see '''[https://ghr.nlm.nih.gov/condition/hepatic-veno-occlusive-disease-with-immunodeficiency Hepatic veno-occlusive disease with immunodeficiency]'''
* '''[https://ghr.nlm.nih.gov/condition/vohwinkel-syndrome Vohwinkel syndrome]'''
* '''[[Von Eulenberg's disease]]''' see '''[https://ghr.nlm.nih.gov/condition/paramyotonia-congenita Paramyotonia congenita]'''
* '''[[von Gierke disease]]''' see '''[https://ghr.nlm.nih.gov/condition/glycogen-storage-disease-type-i Glycogen storage disease type I]'''
* '''[[von Gierke's disease]]''' see '''[https://ghr.nlm.nih.gov/condition/glycogen-storage-disease-type-i Glycogen storage disease type I]'''
* '''[[von Hippel-Lindau disease]]''' see '''[https://ghr.nlm.nih.gov/condition/von-hippel-lindau-syndrome Von Hippel-Lindau syndrome]'''
* '''[https://ghr.nlm.nih.gov/condition/von-hippel-lindau-syndrome Von Hippel-Lindau syndrome]'''
* '''[[von Passow syndrome]]''' see '''[https://ghr.nlm.nih.gov/condition/horner-syndrome Horner syndrome]'''
* '''[[Von Recklenhausen-Applebaum disease]]''' see '''[https://ghr.nlm.nih.gov/condition/hereditary-hemochromatosis Hereditary hemochromatosis]'''
* '''[[von Recklinghausen Disease]]''' see '''[https://ghr.nlm.nih.gov/condition/neurofibromatosis-type-1 Neurofibromatosis type 1]'''
* '''[https://ghr.nlm.nih.gov/condition/von-willebrand-disease Von Willebrand disease]'''
* '''[[von Willebrand disorder]]''' see '''[https://ghr.nlm.nih.gov/condition/von-willebrand-disease Von Willebrand disease]'''
* '''[[von Willebrand factor receptor deficiency]]''' see '''[https://ghr.nlm.nih.gov/condition/bernard-soulier-syndrome Bernard-Soulier syndrome]'''
* '''[[von Willebrand's factor deficiency]]''' see '''[https://ghr.nlm.nih.gov/condition/von-willebrand-disease Von Willebrand disease]'''
* '''[[von Zumbusch psoriasis]]''' see '''[https://ghr.nlm.nih.gov/condition/generalized-pustular-psoriasis Generalized pustular psoriasis]'''
* '''[[Vrolik disease]]''' see '''[https://ghr.nlm.nih.gov/condition/osteogenesis-imperfecta Osteogenesis imperfecta]'''
* '''[[VTLG]]''' see '''[https://ghr.nlm.nih.gov/condition/vitiligo Vitiligo]'''
* '''[[VWS]]''' see '''[https://ghr.nlm.nih.gov/condition/van-der-woude-syndrome Van der Woude syndrome]'''
{{div col end}}
{{genetic diseases}}
{{ni}}

Genetic diseases-V - Revision history

Prab: CSV import

Prab at 21:01, 18 March 2024