Diseases

Name Orphanumber Description XREF(s)
Vitamin K antagonists toxicity or dose selection 413674 Orphanet
Vici syndrome 1493 Vici syndrome is a very rare and severe… Orphanet, ICD-10, OMIM
Vibratory urticaria 493342 Vibratory urticaria is a rare, genetic… Orphanet, ICD-10, OMIM
VEXAS syndrome 596753 A rare autoinflammatory syndrome… Orphanet, OMIM, ICD-10
Very long chain acyl-CoA dehydrogenase deficiency 26793 Very long-chain acyl-CoA dehydrogenase… Orphanet, OMIM, ICD-10
Ventriculomegaly-cystic kidney disease 443988 A rare genetic syndrome with a central… Orphanet, OMIM, ICD-10
Vein of Galen aneurysmal malformation 1053 A congenital vascular malformation… Orphanet, OMIM, MeSH, ICD-10
Vasculitis due to ADA2 deficiency 404553 Vasculitis due to ADA2 deficiency is a… Orphanet, OMIM, ICD-10
Vascular Ehlers-Danlos-polymicrogyria syndrome 636941 Orphanet, OMIM, ICD-10
Vascular Ehlers-Danlos syndrome 286 A rare genetic connective tissue… Orphanet, OMIM, ICD-10
Variant ABeta2M amyloidosis 314652 A rare form of amyloidosis… Orphanet, ICD-10
Van der Woude syndrome 888 Van der Woude syndrome (VWS) is a rare… Orphanet, OMIM, OMIM, OMIM, ICD-10, MeSH
Van den Ende-Gupta syndrome 2460 Van den Ende-Gupta syndrome is a very… Orphanet, ICD-10, OMIM
Vacuolar myopathy with sarcoplasmic reticulum protein aggregates 88635 A rare, genetic vaculolar myopathy… Orphanet, OMIM, ICD-10
VACTERL with hydrocephalus 3412 VACTERL is an acronym for Vertebral… Orphanet, ICD-10, OMIM, OMIM
VACTERL/VATER association 887 VACTERL/VATER is an association of… Orphanet, MeSH, MeSH, MedDRA, ICD-10, OMIM, MedDRA
UV-sensitive syndrome 178338 A rare photodermatosis characterized by… Orphanet, OMIM, OMIM, OMIM, ICD-10
Uveal melanoma 39044 Uveal melanoma is a rare tumor of the… Orphanet, MeSH, MedDRA, OMIM, OMIM, OMIM, ICD-10
Uveal coloboma-cleft lip and palate-intellectual disability 1473 A rare, genetic, multiple congenital… Orphanet, OMIM, ICD-10
USP18 deficiency 481665 A rare genetic neurological disorder… Orphanet, OMIM, ICD-10
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