Browse A-Z | Genetic and Rare Diseases Information Center (GARD) – an NCATS Pro]gram [V]

Browse A-Z | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program

• VACTERL association
• VACTERL association with hydrocephaly - See VACTERL hydrocephaly
• VACTERL association with hydrocephaly, X-linked
• VACTERL hydrocephaly
• Vacuolar cardiomyopathy and myopathy X-linked - See Danon disease
• Vacuolating megalencephalic leukoencephalopathy with subcortical cysts - See Megalencephalic leukoencephalopathy with subcortical cysts
• Vagal paraganglioma - See Glomus vagale tumor
• Vagina, absence of
• Vaginal cancer
• Vagneur Triolle Ripert syndrome
• Valine metabolic defect - See HIBCH deficiency
• Valine transaminase deficiency - See Valinemia
• Valinemia
• Valley fever - See Coccidioidomycosis
• Valproic acid embryopathy - See Fetal valproate syndrome
• Valvar pulmonary stenosis - See Pulmonary valve stenosis
• Valvate pulmonary stenosis - See Pulmonary valve stenosis
• Valvular aortic stenosis - See Aortic valve stenosis
• Valvular heart disease, congenital - See Cardiac valvular dysplasia, X-linked
• Valvular pulmonary stenosis - See Pulmonary valve stenosis
• Valvular pulmonic stenosis - See Pulmonic stenosis
• VAN ASPEREN SYNDROME - See Chromosome 17q11.2 deletion syndrome
• Van Benthem-Driessen-Hanveld syndrome
• Van Bervliet syndrome - See Arthrogryposis IUGR thoracic dystrophy
• Van Biervliet Hendrickx Van Ertbruggen syndrome - See Craniofacial dysostosis arthrogryposis progeroid appearence
• Van Bogaert-Hozay syndrome
• Van Buchem disease - See Hyperostosis corticalis generalisata
• Van Buchem disease type 2
• Van De Berghe Dequeker syndrome - See Ulnar hypoplasia lobster claw deformity of feet
• Van Den Bosch syndrome
• Van Den Ende Brunner syndrome - See Ectrodactyly cardiopathy dysmorphism
• Van den Ende Gupta syndrome - See Marden Walker like syndrome
• Van der Hoeve Halbertsma Waardenburg Gualdi Syndrome - See Waardenburg syndrome
• Van der Hoeve syndrome - See Osteogenesis imperfecta type I
• Van der Woude syndrome
• Van der Woude syndrome 2
• Van Lohuizen syndrome - See Cutis marmorata telangiectatica congenita
• Van Maldergem syndrome - See Cerebro-facio-articular syndrome
• Van Maldergem Wetzburger Verloes syndrome - See Cerebro-facio-articular syndrome
• Vanishing bone disease - See Gorham's disease
• Vanishing white matter disease - See Leukoencephalopathy with vanishing white matter
• Vanishing white matter leukodystrophy - See Leukoencephalopathy with vanishing white matter
• Váradi syndrome - See Orofaciodigital syndrome 6
• Váradi-Papp syndrome - See Orofaciodigital syndrome 6
• Variant A or HHV-6A - See HHV-6 encephalitis
• Variant angina - See Prinzmetal's variant angina
• Variant B or HHV-6B - See HHV-6 encephalitis
• Variant CJD - See Variant Creutzfeldt-Jakob disease
• Variant Creutzfeldt-Jacob disease - See Variant Creutzfeldt-Jakob disease
• Variant Creutzfeldt-Jakob disease
• Variant of Mucha-Habermann disease - See Febrile Ulceronecrotic Mucha-Habermann disease
• Variant phenylketonuria - See Mild phenylketonuria
• Variant PKU - See Mild phenylketonuria
• Varicella Embryopathy - See Congenital varicella syndrome
• Varicella virus antenatal infection - See Congenital varicella syndrome
• Variegate porphyria
• Variola - See Smallpox
• Varioliform gastritis - See Chronic erosive gastritis
• Vascular compression of the duodenum - See Superior mesenteric artery syndrome
• Vascular EDS - See Vascular Ehlers-Danlos syndrome
• Vascular Ehlers-Danlos syndrome
• Vascular hyalinosis
• Vascular purpura - See Henoch-Schonlein purpura
• Vasculitis - not a rare disease
• Vasculitis due to ADA2 deficiency - See Adenosine Deaminase 2 deficiency
• Vasculitis due to DADA2 - See Adenosine Deaminase 2 deficiency
• Vasculitis lymphocytic, nodular - See Lymphocytic vasculitis
• Vasculitis, autoimmune - See Vasculitis - not a rare disease
• Vasoactive intestinal peptide (VIP) tumor - See VIPoma
• Vasoactive intestinal peptide-producing tumor - See VIPoma
• Vasopressin-resistant diabetes insipidus - See Nephrogenic diabetes insipidus
• Vasospastic angina - See Prinzmetal's variant angina
• Vasquez Hurst Sotos syndrome
• VATER association - See VACTERL association
• VBCH - See Hyperostosis corticalis generalisata
• VBCH2 - See Van Buchem disease type 2
• VCFS - See 22q11.2 deletion syndrome
• VCJD - See Variant Creutzfeldt-Jakob disease
• VDEGS - See Marden Walker like syndrome
• VDWS - See Van der Woude syndrome
• vEDS - See Vascular Ehlers-Danlos syndrome
• Vein of Galen aneurysm
• Vein of Galen aneurysm malformation - See Vein of Galen aneurysm
• Velocardiofacial syndrome - See 22q11.2 deletion syndrome
• Velofacioskeletal syndrome
• Velopharyngeal incompetence - See Palatopharyngeal incompetence
• Velopharyngeal insufficiency - See Palatopharyngeal incompetence
• Venezuelan equine encephalitis
• Ventricular extrasystoles perodactyly Robin sequence - See Ventricular extrasystoles with syncopal episodes - perodactyly - Robin sequence
• Ventricular extrasystoles with syncopal episodes - perodactyly - Robin sequence
• Ventricular extrasystoles with syncope, perodactyly, and Robin sequence - See Ventricular extrasystoles with syncopal episodes - perodactyly - Robin sequence
• Ventricular familial preexcitation syndrome - See Wolff-Parkinson-White syndrome - not a rare disease
• Ventricular fibrillation with prolonged QT interval - See Long QT syndrome 1
• Ventricular fibrillation, idiopathic
• Ventricular fibrillation, paroxysmal familial - See Paroxysmal ventricular fibrillation
• Ventricular septal defects
• ventriculoarterial discordance with atrioventricular concordance - See Ventriculoarterial discordance, isolated
• Ventriculoarterial discordance, isolated
• Ventriculomegaly - See Congenital hydrocephalus
• Ventriculo-radial syndrome - See Holt-Oram syndrome
• Verheij syndrome - See Chromosome 8q24.3 deletion syndrome
• Verloes Bourguignon syndrome
• Verloes Gillerot Fryns syndrome - See Male pseudohermaphroditism intellectual disability syndrome, Verloes type
• Verloes syndrome - See Male pseudohermaphroditism intellectual disability syndrome, Verloes type
• Verloes Van Maldergem Marneffe syndrome
• Verloes-David syndrome - See Mesomelia-synostoses syndrome
• Verloes-Gillerot-Fryns syndrome - See Male pseudohermaphroditism intellectual disability syndrome, Verloes type
• Verloove Vanhorick Brubakk syndrome
• Verma Naumoff syndrome - See Short rib-polydactyly syndrome type 3
• Vermiculate atrophoderma, milia, hypotrichosis, trichoepitheliomas, basal cell carcinomas and peripheral vasodilation with cyanosis - See Rombo syndrome
• Vernal keratitis
• Vernal keratoconjunctivitis
• Verner-Morrison syndrome - See WDHA syndrome
• Verrucous epidermal nevus - See Inflammatory linear verrucous epidermal nevus
• Verrucous nevus - See Inflammatory linear verrucous epidermal nevus
• Verrucous nevus acanthokeratolytic
• Vertebral (V), anal (A), cardiac (C), tracheoesophageal (TE), renal (R) and limb (L) anomalies and hydrocephaly - See VACTERL hydrocephaly
• Vertebral artery syndrome - See Wallenberg syndrome
• Vertebral body fusion overgrowth
• Vertebral fusion with carpal coalition - See Spondylocarpotarsal synostosis syndrome
• Vertebrobasilar migraine - See Migraine with brainstem aura
• Vertical talus - See Congenital vertical talus
• Vertical talus, congenital - See Congenital vertical talus
• Very long-chain acyl-CoA dehydrogenase deficiency - See VLCAD deficiency
• Vesicoenteric fistula - See Enterovesical fistula
• Vessel’s syndrome - See Proximal symphalangism
• Vestibular schwannoma - See Acoustic neuroma
• Vestibulocerebellar disorder with predominant ocular signs - See Nystagmus 4, congenital, autosomal dominant
• Vestibulocochlear dysfunction, progressive
• VGAM - See Vein of Galen aneurysm
• VHL - See Von Hippel-Lindau disease
• VHL syndrome - See Von Hippel-Lindau disease
• VI nerve palsy - See Sixth nerve palsy
• Vibratory angioedema - See Vibratory urticaria
• Vibratory urticaria
• Vibrio cholerae infection - See Cholera
• Vibrio vulnificus infection
• Vici syndrome
• Viljoen Kallis Voges syndrome
• Viljoen Smart syndrome - See Microphthalmia syndromic 8
• Vincent's gingivitis - See Acute necrotizing ulcerative gingivitis
• Vincent's infection - See Acute necrotizing ulcerative gingivitis
• Vincent's stomatitis - See Acute necrotizing ulcerative gingivitis
• VIPoma
• Vipoma Syndrome - See WDHA syndrome
• VIP-secreting tumor - See VIPoma
• Viral hemorrhagic fever
• Viral hepatitis non-A,-B,-C,-D,-E - See Non-A-E hepatitis
• Virilizing ovarian tumor
• Virus associated hemophagocytic syndrome
• Visceral heterotaxy - See Heterotaxy
• Visceral leishmaniasis (subtype) - See Leishmaniasis
• Visceral myopathy - familial external ophthalmoplegia - See Familial visceral myopathy with external ophthalmoplegia
• Visceral myopathy familial - See Megaduodenum and/or megacystis
• Visceral myopathy, familial, with external ophthalmoplegia - See Familial visceral myopathy with external ophthalmoplegia
• Visceral neuromyopathy familial with pseudoobstruction megaduodenum barrett esophagus and cardiac abnormalities - See Mungan syndrome
• Visceral neuropathy familial
• Visceral steatosis
• Visual amnesia - See Agnosia
• Visual pathway and hypothalamic glioma, childhood
• Visual snow - See Visual snow syndrome
• Visual snow syndrome
• Vitamin A Deficiency - See Keratomalacia
• Vitamin B1 deficiency - See Beriberi
• Vitamin B12-responsive methylmalonic acidemia
• Vitamin B12-responsive methylmalonic acidemia type cblA - See Methylmalonic aciduria, cblA type
• Vitamin B12-responsive methylmalonic acidemia type cblB - See Methylmalonic aciduria, cblB type
• Vitamin B12-responsive methylmalonic aciduria - See Vitamin B12-responsive methylmalonic acidemia
• Vitamin B12-responsive methylmalonic aciduria type cblA - See Methylmalonic aciduria, cblA type
• Vitamin B12-responsive methylmalonic aciduria, type cblB - See Methylmalonic aciduria, cblB type
• Vitamin B6 deficiency - See Pyridoxine deficiency
• Vitamin B6-dependent seizures - See Pyridoxine-dependent epilepsy
• Vitamin C deficiency - See Scurvy
• Vitamin D deficiency disease - See Rickets
• Vitamin deficiency, B6 - See Pyridoxine deficiency
• Vitamin D-Resistant Rickets, X-linked - See X-linked hypophosphatemia
• Vitamin K antagonists embryofetopathy - See Warfarin syndrome
• Vitamin K-antagonist embryofetopathy - See Warfarin syndrome
• Vitamin K-antagonist embryopathy - See Warfarin syndrome
• Vitamin-D deficiency rickets - See Rickets
• Vitelliform macular dystrophy type 2 - See Best vitelliform macular dystrophy
• Vitelliform macular dystrophy, adult-onset - See Adult-onset vitelliform macular dystrophy
• Vitelliform macular dystrophy, atypical - See Macular dystrophy, atypical vitelliform
• Vitiliginous choroiditis - See Birdshot chorioretinopathy
• Vitiligo - not a rare disease
• Vitiligo vulgaris, cleft palate, somatic and psychomotor retardation and facial dysmorphism - See Schrander-Stumpel Theunissen Hulsmans syndrome
• Vitiligo, psychomotor retardation, cleft palate and facial dysmorphism - See Schrander-Stumpel Theunissen Hulsmans syndrome
• Vitreoretinal degeneration
• Vitreoretinal degeneration, Snowflake type - See Snowflake vitreoretinal degeneration
• Vitreoretinochoroidopathy dominant - See Autosomal dominant vitreoretinochoroidopathy
• Vitritis - See Pars planitis
• Vitsala - See Kifafa seizure disorder
• VKC - See Vernal keratoconjunctivitis
• VKH disease - See Vogt-Koyanagi-Harada disease
• VKH syndrome - See Vogt-Koyanagi-Harada disease
• VLCAD deficiency
• VLCADD - See VLCAD deficiency
• VLDLRCH - See Dysequilibrium syndrome
• VMD1 - See Macular dystrophy, atypical vitelliform
• VMD2 - See Best vitelliform macular dystrophy
• Vocal cord dysfunction familial
• VODI - See Hepatic venoocclusive disease with immunodeficiency
• Vogt Spielmeyer disease - See Neuronal ceroid lipofuscinosis 3
• Vogt-Koyanagi-Harada disease
• Vogt-Koyanagi-Harada syndrome - See Vogt-Koyanagi-Harada disease
• Vohwinkel syndrome
• Voiding dysfunction and polycystic ovaries - See Fowler's syndrome
• Volcke Soekarman syndrome - See Macrocephaly-short stature-paraplegia syndrome
• Volcke-Soekarman syndrome - See Macrocephaly-short stature-paraplegia syndrome
• Volubilis syndrome - See Morning glory syndrome
• Von Bogaert-Bertrand disease - See Canavan disease
• Von Economo’s disease - See Encephalitis lethargica
• Von Eulenburg paramyotonia congenita - See Paramyotonia congenita
• Von Gierke disease - See Glycogen storage disease type 1A
• Von Hippel-Lindau disease - See Von Hippel-Lindau disease
• Von Hippel-Lindau disease
• Von Hippel-Lindau syndrome - See Von Hippel-Lindau disease
• Von Recklinghausen disease - See Neurofibromatosis type 1
• Von Voss Cherstvoy syndrome - See DK phocomelia syndrome
• Von Willebrand disease - not a rare disease
• Von Willebrand disease, platelet type - See Pseudo-Von Willebrand disease
• Von Willebrand factor receptor deficiency - See Giant platelet syndrome
• Von Willebrand factor, deficiency - See Von Willebrand disease - not a rare disease
• Voorhoeve disease - See Osteopathia striata cranial sclerosis
• VP - See Variegate porphyria
• VRCP autosomal dominant - See Autosomal dominant vitreoretinochoroidopathy
• Vrolik disease - See Osteogenesis imperfecta
• Vrolik type of osteogenesis imperfecta - See Osteogenesis imperfecta type II
• Vulvar cancer
• Vulvar dysesthesia localized in the vestibule - See Vulvar Vestibulitis Syndrome
• Vulvar Vestibulitis Syndrome
• VVS - See Vulvar Vestibulitis Syndrome
• VWD - See Von Willebrand disease - not a rare disease
• VWS - See Van der Woude syndrome
• VWS2 - See Van der Woude syndrome 2