Diseases

Name Orphanumber Description XREF(s)
Von Willebrand disease type 2A 166084 A subtype of type 2 von Willebrand… Orphanet, ICD-10, OMIM
Von Willebrand disease type 2M 166090 A subtype of type 2 von Willebrand… Orphanet, OMIM, ICD-10
Von Willebrand disease type 2B 166087 A subtype of type 2 von Willebrand… Orphanet, ICD-10, OMIM
Von Willebrand disease type 2N 166093 A subtype of type 2 von Willebrand… Orphanet, ICD-10, OMIM
Von Willebrand disease type 1 166078 A form of von Willebrand disease (VWD)… Orphanet, MeSH, OMIM, ICD-10
Von Willebrand disease type 3 166096 A form of von Willebrand disease (VWD)… Orphanet, MeSH, ICD-10, OMIM
Voriconazole toxicity 240921 Orphanet
VPS11-related autosomal recessive hypomyelinating leukodystrophy 466934 A rare genetic leukodystrophy… Orphanet, ICD-10, OMIM
Waardenburg syndrome type 1 894 A subtype of Waardenburg syndrome (WS)… Orphanet, OMIM, ICD-10
Waardenburg syndrome type 2 895 An autosomal dominant subtype of… Orphanet, OMIM, OMIM, OMIM, OMIM, OMIM, OMIM, MeSH, ICD-10
Waardenburg syndrome type 3 896 A very rare subtype of Waardenburg… Orphanet, OMIM, ICD-10
Waardenburg-Shah syndrome 897 Waardenburg-Shah syndrome (WSS), also… Orphanet, OMIM, OMIM, OMIM, ICD-10
Wagner disease 898 Wagner disease is a rare hereditary… Orphanet, MedDRA, MeSH, ICD-10, OMIM
WAGR syndrome 893 A rare genetic disorder characterized… Orphanet, MeSH, MeSH, ICD-10, OMIM, OMIM
Waldenström macroglobulinemia 33226 Waldenström macroglobulinemia (WM) is… Orphanet, MeSH, MedDRA, OMIM, OMIM, ICD-10
Walker-Warburg syndrome 899 A rare form of congenital muscular… Orphanet, OMIM, MeSH, OMIM, OMIM, OMIM, OMIM, OMIM, OMIM, ICD-10, OMIM, OMIM, OMIM, OMIM, OMIM, OMIM, OMIM
WARS2-related combined oxidative phosphorylation defect 572798 A rare mitochondrial oxidative… Orphanet, OMIM, ICD-10
Warsaw breakage syndrome 280558 A rare genetic multiple congenital… Orphanet, OMIM, ICD-10
Weaver syndrome 3447 Weaver syndrome (WVS) is a rare,… Orphanet, OMIM, ICD-10, OMIM, MeSH, OMIM
Weill-Marchesani syndrome 3449 Weill-Marchesani syndrome (WMS) is a… Orphanet, MedDRA, OMIM, OMIM, OMIM, MeSH, ICD-10
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