List of rare diseases-V
From WikiMD's Food, Medicine & Wellness Encyclopedia
NIH genetic and rare disease info[edit source]
List of rare diseases-V is a rare disease.
- VACTERL association
- VACTERL association with hydrocephaly
- VACTERL association with hydrocephaly, X-linked
- VACTERL hydrocephaly
- Vacuolar cardiomyopathy and myopathy X-linked
- Vacuolating megalencephalic leukoencephalopathy with subcortical cysts
- Vagal paraganglioma
- Vagina, absence of
- Vaginal cancer
- Vagneur Triolle Ripert syndrome
- Valine metabolic defect
- Valine transaminase deficiency
- Valinemia
- Valley fever
- Valproic acid embryopathy
- Valvar pulmonary stenosis
- Valvate pulmonary stenosis
- Valvular aortic stenosis
- Valvular heart disease, congenital
- Valvular pulmonary stenosis
- Valvular pulmonic stenosis
- VAN ASPEREN SYNDROME
- Van Benthem-Driessen-Hanveld syndrome
- Van Bervliet syndrome
- Van Biervliet Hendrickx Van Ertbruggen syndrome
- Van Bogaert-Hozay syndrome
- Van Buchem disease
- Van Buchem disease type 2
- Van De Berghe Dequeker syndrome
- Van Den Bosch syndrome
- Van Den Ende Brunner syndrome
- Van den Ende Gupta syndrome
- Van der Hoeve Halbertsma Waardenburg Gualdi Syndrome
- Van der Hoeve syndrome
- Van der Woude syndrome
- Van der Woude syndrome 2
- Van Lohuizen syndrome
- Van Maldergem syndrome
- Van Maldergem Wetzburger Verloes syndrome
- Vanishing bone disease
- Vanishing white matter disease
- Vanishing white matter leukodystrophy
- Váradi syndrome
- Váradi-Papp syndrome
- Variant A or HHV-6A
- Variant angina
- Variant B or HHV-6B
- Variant CJD
- Variant Creutzfeldt-Jacob disease
- Variant Creutzfeldt-Jakob disease
- Variant of Mucha-Habermann disease
- Variant phenylketonuria
- Variant PKU
- Varicella Embryopathy
- Varicella virus antenatal infection
- Variegate porphyria
- Variola
- Varioliform gastritis
- Vascular compression of the duodenum
- Vascular EDS
- Vascular Ehlers-Danlos syndrome
- Vascular hyalinosis
- Vascular purpura
- Vasculitis- not a rare disease.
- Vasculitis due to ADA2 deficiency
- Vasculitis due to DADA2
- Vasculitis lymphocytic, nodular
- Vasculitis, autoimmune- not a rare disease.
- Vasoactive intestinal peptide (VIP) tumor
- Vasoactive intestinal peptide-producing tumor
- Vasopressin-resistant diabetes insipidus
- Vasospastic angina
- Vasquez Hurst Sotos syndrome
- VATER association
- VBCH
- VBCH2
- VCFS
- VCJD
- VDEGS
- VDWS
- vEDS
- Vein of Galen aneurysm
- Vein of Galen aneurysm malformation
- Velocardiofacial syndrome
- Velofacioskeletal syndrome
- Velopharyngeal incompetence
- Velopharyngeal insufficiency
- Venezuelan equine encephalitis
- Ventricular extrasystoles perodactyly Robin sequence
- Ventricular extrasystoles with syncopal episodes - perodactyly - Robin sequence
- Ventricular extrasystoles with syncope, perodactyly, and Robin sequence
- Ventricular familial preexcitation syndrome- not a rare disease.
- Ventricular fibrillation with prolonged QT interval
- Ventricular fibrillation, idiopathic
- Ventricular fibrillation, paroxysmal familial
- Ventricular septal defects
- ventriculoarterial discordance with atrioventricular concordance
- Ventriculoarterial discordance, isolated
- Ventriculomegaly
- Ventriculo-radial syndrome
- Verheij syndrome
- Verloes Bourguignon syndrome
- Verloes Gillerot Fryns syndrome
- Verloes syndrome
- Verloes Van Maldergem Marneffe syndrome
- Verloes-David syndrome
- Verloes-Gillerot-Fryns syndrome
- Verloove Vanhorick Brubakk syndrome
- Verma Naumoff syndrome
- Vermiculate atrophoderma, milia, hypotrichosis, trichoepitheliomas, basal cell carcinomas and peripheral vasodilation with cyanosis
- Vernal keratitis
- Vernal keratoconjunctivitis
- Verner-Morrison syndrome
- Verrucous epidermal nevus
- Verrucous nevus
- Verrucous nevus acanthokeratolytic
- Vertebral (V), anal (A), cardiac (C), tracheoesophageal (TE), renal (R) and limb (L) anomalies and hydrocephaly
- Vertebral artery syndrome
- Vertebral body fusion overgrowth
- Vertebral fusion with carpal coalition
- Vertebrobasilar migraine
- Vertical talus
- Vertical talus, congenital
- Very long-chain acyl-CoA dehydrogenase deficiency
- Vesicoenteric fistula
- Vessel’s syndrome
- Vestibular schwannoma
- Vestibulocerebellar disorder with predominant ocular signs
- Vestibulocochlear dysfunction, progressive
- VGAM
- VHL
- VHL syndrome
- VI nerve palsy
- Vibratory angioedema
- Vibratory urticaria
- Vibrio cholerae infection
- Vibrio vulnificus infection
- Vici syndrome
- Viljoen Kallis Voges syndrome
- Viljoen Smart syndrome
- Vincent's gingivitis
- Vincent's infection
- Vincent's stomatitis
- VIPoma
- Vipoma Syndrome
- VIP-secreting tumor
- Viral hemorrhagic fever
- Viral hepatitis non-A,-B,-C,-D,-E
- Virilizing ovarian tumor
- Virus associated hemophagocytic syndrome
- Visceral heterotaxy
- Visceral leishmaniasis (subtype)
- Visceral myopathy - familial external ophthalmoplegia
- Visceral myopathy familial
- Visceral myopathy, familial, with external ophthalmoplegia
- Visceral neuromyopathy familial with pseudoobstruction megaduodenum barrett esophagus and cardiac abnormalities
- Visceral neuropathy familial
- Visceral steatosis
- Visual amnesia
- Visual pathway and hypothalamic glioma, childhood
- Visual snow
- Visual snow syndrome
- Vitamin A Deficiency
- Vitamin B1 deficiency
- Vitamin B12-responsive methylmalonic acidemia
- Vitamin B12-responsive methylmalonic acidemia type cblA
- Vitamin B12-responsive methylmalonic acidemia type cblB
- Vitamin B12-responsive methylmalonic aciduria
- Vitamin B12-responsive methylmalonic aciduria type cblA
- Vitamin B12-responsive methylmalonic aciduria, type cblB
- Vitamin B6 deficiency
- Vitamin B6-dependent seizures
- Vitamin C deficiency
- Vitamin D deficiency disease
- Vitamin deficiency, B6
- Vitamin D-Resistant Rickets, X-linked
- Vitamin K antagonists embryofetopathy
- Vitamin K-antagonist embryofetopathy
- Vitamin K-antagonist embryopathy
- Vitamin-D deficiency rickets
- Vitelliform macular dystrophy type 2
- Vitelliform macular dystrophy, adult-onset
- Vitelliform macular dystrophy, atypical
- Vitiliginous choroiditis
- Vitiligo- not a rare disease.
- Vitiligo vulgaris, cleft palate, somatic and psychomotor retardation and facial dysmorphism
- Vitiligo, psychomotor retardation, cleft palate and facial dysmorphism
- Vitreoretinal degeneration
- Vitreoretinal degeneration, Snowflake type
- Vitreoretinochoroidopathy dominant
- Vitritis
- Vitsala
- VKC
- VKH disease
- VKH syndrome
- VLCAD deficiency
- VLCADD
- VLDLRCH
- VMD1
- VMD2
- Vocal cord dysfunction familial
- VODI
- Vogt Spielmeyer disease
- Vogt-Koyanagi-Harada disease
- Vogt-Koyanagi-Harada syndrome
- Vohwinkel syndrome
- Voiding dysfunction and polycystic ovaries
- Volcke Soekarman syndrome
- Volcke-Soekarman syndrome
- Volubilis syndrome
- Von Bogaert-Bertrand disease
- Von Economo’s disease
- Von Eulenburg paramyotonia congenita
- Von Gierke disease
- Von Hippel-Lindau disease
- Von Hippel-Lindau disease
- Von Hippel-Lindau syndrome
- Von Recklinghausen disease
- Von Voss Cherstvoy syndrome
- Von Willebrand disease- not a rare disease.
- Von Willebrand disease, platelet type
- Von Willebrand factor receptor deficiency
- Von Willebrand factor, deficiency- not a rare disease.
- Voorhoeve disease
- VP
- VRCP autosomal dominant
- Vrolik disease
- Vrolik type of osteogenesis imperfecta
- Vulvar cancer
- Vulvar dysesthesia localized in the vestibule
- Vulvar Vestibulitis Syndrome
- VVS
- VWD- not a rare disease.
- VWS
- VWS2
NIH genetic and rare disease info[edit source]
List of rare diseases-V is a rare disease.
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