List of rare diseases-V

NIH genetic and rare disease info

• NIH info on List of rare diseases-V

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

• NIH info on List of rare diseases-V

List of rare diseases-V is a rare disease.