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207 Result(s)
- v-AT
- VACTERL association
- VACTERL with hydrocephalus
- VACTERL/VATER association
- Vacuolar aggregate myopathy
- Vacuolar myopathy with sarcoplasmic reticulum protein aggregates
- Vacuolar sorting protein 45 deficiency
- Vacuolating megalencephalic leukoencephalopathy with subcortical cysts
- Vaginal atresia
- Vaginal carcinoma
- Vaginal germ cell cancer
- Vaginal germ cell malignant tumor
- Vaginal malignant epithelial tumor
- VAHS
- Valine metabolic defect
- Valley fever
- Valproic acid embryopathy
- Valvular pulmonary stenosis
- Van Benthem-Driessen-Hanveld syndrome
- Van Bogaert disease
- Van Bogaert encephalitis
- Van Buchem disease
- Van den Berghe-Dequecker syndrome
- Van den Bosch syndrome
- Van den Ende-Gupta syndrome
- Van der Hoeve syndrome
- Van der Knaap syndrome
- Van der Woude syndrome
- Van Maldergem syndrome
- Vanishing bone disease
- Vanishing testes syndrome
- Vanishing testis syndrome
- Vaquez disease
- Variably protease-sensitive prionopathy
- Variant ABeta2M amyloidosis
- Variant Creutzfeldt-Jakob disease
- Variant MCJ
- Variant of GBS
- Variant of Guillain-Barré syndrome
- Variant phenylketonuria
- Variant PKU
- Variegate porphyria
- Vasa previa
- Vascular EDS
- Vascular EDS with polymicrogyria
- Vascular Ehlers-Danlos syndrome
- Vascular Ehlers-Danlos-polymicrogyria syndrome
- Vascular intermediate tumors
- Vascular locally aggressive tumors
- Vasculitis
- Vasculitis-autoinflammation-immunodeficiency- hematologic defects syndrome
- Vasoproliferative tumor of the ocular fundus
- Vasoproliferative tumor of the retina
- VATER association
- Vater-like syndrome with pulmonary hypertension, abnormal ears and growth deficiency
- VATS
- VCAN-related vitreoretinopathy
- vCJD
- VCPDM
- VDDI
- VDDR II
- VDDR-I
- VDEGS
- VDRR II
- vEDS
- Vegetant intravascular hemangioendothelioma
- Vegetative pyoderma gangrenosum
- VEGFC-related congenital primary lymphedema
- Vein of Galen aneurysmal malformation
- Vein of Galen arteriovenous malformations
- Velo-facial-skeletal syndrome
- Velocardiofacial syndrome
- Venezuelan hemorrhagic fever
- Venous cervical rib syndrome
- Venous costoclavicular syndrome
- Venous hyperabduction syndrome
- Venous malformation of the spleen
- Venous malformations with glomus cells
- Venous scalenus anticus syndrome
- Venous thoracic outlet compression syndrome
- Venous thoracic outlet syndrome
- Venous TOS
- Ventilator-induced diaphragmatic dysfunction
- Ventricular extrasystoles with syncopal episodes-perodactyly-Robin sequence syndrome
- Ventricular inversion
- Ventricular septal defect with aortic insufficiency
- Ventriculoarterial and atrioventricular discordance
- Ventriculoarterial discordance with atrioventricular concordance
- Ventriculomegaly-cystic kidney disease
- VEOS
- Verloes-Bourguignon syndrome
- Verloes-David syndrome
- Verloes-Gillerot-Fryns syndrome
- Verloes-Van Maldergem-de Marneffe syndrome
- Verloove Vanhorick-Brubakk syndrome
- Vernal keratoconjunctivitis
- Verner-Morrison syndrome
- Verrucous hemangioma
- Verrucous nevus
- Verruga peruana
- Vertebral defects-anal atresia-cardiac defects-tracheo-esophageal fistula-renal anomalies-limb abnormalities association
- Very early-onset schizophrenia
- Very long chain acyl-CoA dehydrogenase deficiency
- Vesicourachal diverticulum
- Vestibular schwannoma
- VEXAS syndrome
- VHL
- Vibratory angioedema/urticaria
- Vibratory urticaria
- Vici syndrome
- VIDD
- Viljoen-Kallis-Voges syndrome
- Viljoen-Smart syndrome
- VIN
- VIP-secreting tumor
- VIPoma
- Viral hemorrhagic fever
- Viral myositis
- Virginal breast hypertrophy
- Virilizing ovarian tumor
- Virus-associated hemophagocytic syndrome
- Virus-associated trichodysplasia spinulosa
- Visceral arteriovenous malformation
- Visceral calciphylaxis
- Visceral fibromuscular dysplasia
- Visceral heterotaxy
- Visceral malformation of the liver, biliary tract, pancreas or spleen
- Visceral myopathy-familial external ophthalmoplegia syndrome
- Visceral neuropathy-brain anomalies-facial dysmorphism-developmental delay syndrome
- Visible and exudative idiopathic juxtafoveolar retinal telangiectasis
- Visual snow syndrome
- Vitamin B12- and folate-independent constitutional megaloblastic anemia
- Vitamin B12-responsive methylmalonic acidemia
- Vitamin B12-responsive methylmalonic acidemia type cblA
- Vitamin B12-responsive methylmalonic acidemia type cblB
- Vitamin B12-responsive methylmalonic acidemia, type cblDv2
- Vitamin B12-responsive methylmalonic aciduria
- Vitamin B12-responsive methylmalonic aciduria type cblA
- Vitamin B12-responsive methylmalonic aciduria, type cblB
- Vitamin B12-responsive methylmalonic aciduria, type cblDv2
- Vitamin B12-unresponsive methylmalonic acidemia
- Vitamin B12-unresponsive methylmalonic acidemia type mut-
- Vitamin B12-unresponsive methylmalonic acidemia type mut0
- Vitamin B12-unresponsive methylmalonic aciduria
- Vitamin B12-unresponsive methylmalonic aciduria type mut-
- Vitamin B12-unresponsive methylmalonic aciduria type mut0
- Vitamin B6-dependent seizures
- Vitamin D dependent rickets type I
- Vitamin D-dependency type I
- Vitamin D-dependent rickets type II
- Vitamin D-resistant rickets type II
- Vitamin K antagonist embryofetopathy
- Vitamin K antagonist embryopathy
- Vitelliform macular dystrophy type 2
- Vitiliginous choroiditis
- Vitreoretinal degeneration, Wagner type
- Vitreoretinopathy
- VLCAD deficiency
- VLCADD
- vLINCL
- vLINCL
- VMC
- VMCKD
- VMCM
- VMGLOM
- Vocal cord and pharyngeal distal myopathy
- VODI syndrome
- Vogt-Koyanagi-Harada disease
- Vohwinkel syndrome
- Vohwinkel syndrome with ichthyosis
- Volcke-Soekarman syndrome
- Von Economo encephalitis
- Von Gierke disease
- Von Hippel-Lindau disease
- Von Hippel-Lindau syndrome
- Von Hippel-Lindau-dependent polycythemia
- Von Meyenburg complexes disease
- Von Recklinghausen disease
- Von Recklinghausen disease due to NF1 mutation or intragenic deletion
- Von Voss-Cherstvoy syndrome
- Von Willebrand disease
- Von Willebrand disease type 1
- Von Willebrand disease type 2
- Von Willebrand disease type 2A
- Von Willebrand disease type 2B
- Von Willebrand disease type 2M
- Von Willebrand disease type 2N
- Von Willebrand disease type 3
- VPS11-related autosomal recessive hypomyelinating leukodystrophy
- VPS11-related autosomal recessive hypomyelinating leukoencephalopathy
- VPS45 deficiency
- VPTR
- VSD with aortic insufficiency
- VTOS
- Vulvar adenocarcinoma
- Vulvar basal cell carcinoma
- Vulvar carcinoma
- Vulvar intraepithelial neoplasia
- Vulvar intraepithelial tumor
- Vulvar squamous cell carcinoma
- Vulvovaginal gingival syndrome
- Vulvovaginal rhabdomyosarcoma
- Vuopala disease
- VWS
- Váradi syndrome
- Váradi-Papp syndrome
- Västerbotten dystrophy