Diseases

Name Orphanumber Description XREF(s)
Van der Woude syndrome 888 Van der Woude syndrome (VWS) is a rare… Orphanet, OMIM, OMIM, OMIM, ICD-10, MeSH
Variant ABeta2M amyloidosis 314652 A rare form of amyloidosis… Orphanet, ICD-10
Vascular Ehlers-Danlos syndrome 286 A rare genetic connective tissue… Orphanet, OMIM, ICD-10
Vascular Ehlers-Danlos-polymicrogyria syndrome 636941 Orphanet, OMIM, ICD-10
Vasculitis due to ADA2 deficiency 404553 Vasculitis due to ADA2 deficiency is a… Orphanet, OMIM, ICD-10
Vein of Galen aneurysmal malformation 1053 A congenital vascular malformation… Orphanet, OMIM, MeSH, ICD-10
Ventriculomegaly-cystic kidney disease 443988 A rare genetic syndrome with a central… Orphanet, OMIM, ICD-10
Very long chain acyl-CoA dehydrogenase deficiency 26793 Very long-chain acyl-CoA dehydrogenase… Orphanet, OMIM, ICD-10
VEXAS syndrome 596753 A rare autoinflammatory syndrome… Orphanet, OMIM, ICD-10
Vibratory urticaria 493342 Vibratory urticaria is a rare, genetic… Orphanet, ICD-10, OMIM
Vici syndrome 1493 Vici syndrome is a very rare and severe… Orphanet, ICD-10, OMIM
Vitamin K antagonists toxicity or dose selection 413674 Orphanet
Vitamin B12-responsive methylmalonic acidemia, type cblDv2 308442 Orphanet, ICD-10, OMIM
Vitamin B12-responsive methylmalonic acidemia type cblA 79310 Orphanet, MeSH, ICD-10, OMIM
Vitamin B12-responsive methylmalonic acidemia type cblB 79311 Orphanet, MeSH, OMIM, ICD-10
Vitamin B12-unresponsive methylmalonic acidemia type mut- 79312 Vitamin B12-unresponsive methylmalonic… Orphanet, OMIM, ICD-10
Vitamin B12-unresponsive methylmalonic acidemia type mut0 289916 Vitamin B12-unresponsive methylmalonic… Orphanet, ICD-10, OMIM
Vocal cord and pharyngeal distal myopathy 600 Vocal cord and pharyngeal distal… Orphanet, OMIM, ICD-10
Vogt-Koyanagi-Harada disease 3437 Vogt-Koyanagi-Harada disease is a… Orphanet, ICD-10, ICD-10
Von Hippel-Lindau disease 892 Von Hippel-Lindau disease (VHL) is a… Orphanet, OMIM, MeSH, MedDRA, ICD-10