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Diseases

Genetic and Rare Diseases Information Center (GARD)

Search for Rare or Genetic Diseases


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Diseases Beginning With V

The purpose of the Rare Diseases and Related Terms list is to distribute information; although the list is updated regularly, it should not be used as a reference or guarantee that a condition is rare. The prevalence of a rare disease is usually an estimate and may change over time. A rare (or orphan) disease is generally considered to have a prevalence of fewer than 200,000 affected individuals in the United States.

* This symbol indicates that a condition is not rare but is one for which a question has been answered by the GARD Information Center.

* 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
* Vacuolar myopathy
* Vacuolating megalencephalic leukoencephalopathy with subcortical cysts - See Megalencephalic leukoencephalopathy with subcortical cysts
* Vagal paraganglioma - See Glomus vagale tumors
* Vagina, absence of
* Vaginal cancer
* Vagneur Triolle Ripert syndrome
* Valine transaminase deficiency - See Valinemia
* Valinemia
* Valley fever - See Coccidioidomycosis
* Valproic acid embryopathy - See Fetal valproate syndrome
* Valproic acid fetal effects from - 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 Allen Myhre 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 Woude syndrome
* Van der Woude syndrome 2
* Van Goethem syndrome - See Radio-digito-facial dysplasia
* Van Maldergem syndrome - See Van Maldergem Wetzburger Verloes syndrome
* Van Maldergem Wetzburger Verloes syndrome
* Van Regemorter Pierquin Vamos syndrome
* Vanishing bone disease - See Gorham's disease
* Vanishing testes - See Anorchia
* Varadi-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
* Varicella Embryopathy - See Congenital varicella syndrome
* Varicella virus antenatal infection - See Varicella virus antenatal infection
* Varicella virus antenatal infection
* Variegate porphyria
* Variola - See Smallpox
* Varioliform gastritis - See Chronic erosive gastritis
* Vascular compression of the duodenum - See Superior mesenteric artery syndrome
* Vascular hyalinosis
* Vascular malposition
* Vascular purpura - See Henoch-Schonlein purpura
*   Vasculitis
* Vasculitis lymphocytic, nodular - See Lymphocytic vasculitis
*   Vasculitis, autoimmune - See Vasculitis
* Vasoactive intestinal peptide (VIP) tumor - See VIPoma
* Vasoactive intestinal peptide-producing tumor - See VIPoma
* Vasopressin-resistant diabetes insipidus - See Nephrogenic diabetes insipidus
* 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
* 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
* Venencie Powell Gordon Winkelmann syndrome
* 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
* 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
* Ventriculo-arterial discordance, isolated
* Ventriculomegaly - See Hydrocephalus
* Ventriculo-radial syndrome - See Holt-Oram syndrome
* Ventruto Digirolamo Festa syndrome
* Verbal apraxia - See Apraxia
* 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 posterior lumbosacral blepharoptosis
* Vertebral fusion with carpal coalition - See Spondylocarpotarsal synostosis syndrome
* Vertebrobasilar migraine - See Basilar migraine
* Vertical talus, congenital
* Very long-chain acyl-CoA dehydrogenase deficiency - See VLCAD deficiency
* Vesicles, celosomia, short neck, microcornea and dextrocardia - See Van Allen Myhre syndrome
* Vessel’s syndrome - See Cushing's 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
* Vibrio cholerae infection - See Cholera
* Vibrio vulnificus infection
* Vici syndrome
* Viljoen Kallis Voges syndrome
* Viljoen Smart syndrome - See Microphthalmia syndromic 8
* Viljoen Winship syndrome
* 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
* 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 syndrome
* Vitamin A Deficiency - See Keratomalacia
* Vitamin A embryopathy
* Vitamin B1 deficiency - See Beriberi
* 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 Hypophosphatemic rickets
* 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
*   Vitiligo
* Vitiligo mental retardation facial dysmorphism uremia
* 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
* Vitritis - See Pars planitis
* Vitsala - See Kifafa seizure disorder
* VKC - See Vernal keratoconjunctivitis
* VKH syndrome - See Vogt-Koyanagi-Harada syndrome
* 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 Batten disease
* Vogt-Koyanagi-Harada syndrome
* Vohwinkel syndrome
* Voiding dysfunction and polycystic ovaries - See Fowler's syndrome
* Volcke Soekarman syndrome - See Macrocephaly, mental retardation, short stature, spastic paraplegia and CNS malformations
* 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 Mayer Rokitansky Kuster anomaly - See Mayer-Rokitansky-Kuster-Hauser syndrome
* Von Recklinghausen disease - See Neurofibromatosis type 1
* Von Voss Cherstvoy syndrome - See DK phocomelia syndrome
*   Von Willebrand 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
* VP - See Variegate porphyria
* VRCP autosomal dominant - See Vitreoretinochoroidopathy dominant
* Vrolik disease - See Osteogenesis imperfecta
* Vrolik type of osteogenesis imperfecta - See Osteogenesis imperfecta type 2A
* VSR syndrome - See Herrmann Opitz arthrogryposis syndrome
* 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
* VWS - See Van der Woude syndrome
* VWS2 - See Van der Woude syndrome 2