Diseases

Name Orphanumber Description XREF(s)
Wilson-Turner syndrome 3459 Wilson-Turner syndrome (WTS) is a very… Orphanet, ICD-10, OMIM
Wilson disease 905 A rare genetic disorder of copper… Orphanet, MeSH, MedDRA, ICD-10, OMIM
Williams syndrome 904 A rare genetic multisystemic… Orphanet, ICD-10, MedDRA, OMIM, MeSH
Wiedemann-Steiner syndrome 319182 A rare, genetic multiple congenital… Orphanet, ICD-10, OMIM
Wiedemann-Rautenstrauch syndrome 3455 A rare multiple congenital anomalies/… Orphanet, MeSH, OMIM, ICD-10
White-Sutton syndrome 468678 A rare, genetic, syndromic intellectual… Orphanet, ICD-10, OMIM
White sponge nevus 171723 White sponge nevus (WSN) is a rare and… Orphanet, ICD-10, OMIM, OMIM
Whipple disease 3452 A rare chronic infectious disorder in… Orphanet, ICD-10, MeSH, MeSH, MedDRA, ICD-10
WHIM syndrome 51636 WHIM (warts, hypogammaglobulinemia,… Orphanet, MeSH, OMIM, ICD-10
Werner syndrome 902 Werner syndrome (WS) is a rare… Orphanet, MeSH, MedDRA, OMIM, ICD-10
Well-differentiated liposarcoma 99971 Well-differentiated liposarcoma (WDLS… Orphanet, ICD-10
Weissenbacher- Zweymuller syndrome 3450 Weissenbacher-Zweymuller syndrome (WZS… Orphanet, ICD-10, OMIM
Weill-Marchesani syndrome 3449 Weill-Marchesani syndrome (WMS) is a… Orphanet, MedDRA, OMIM, OMIM, OMIM, MeSH, ICD-10
Weaver syndrome 3447 Weaver syndrome (WVS) is a rare,… Orphanet, OMIM, ICD-10, OMIM, MeSH, OMIM
Warsaw breakage syndrome 280558 A rare genetic multiple congenital… Orphanet, OMIM, ICD-10
WARS2-related combined oxidative phosphorylation defect 572798 A rare mitochondrial oxidative… Orphanet, 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
Waldenström macroglobulinemia 33226 Waldenström macroglobulinemia (WM) is… Orphanet, MeSH, MedDRA, OMIM, OMIM, ICD-10
WAGR syndrome 893 A rare genetic disorder characterized… Orphanet, MeSH, MeSH, ICD-10, OMIM, OMIM
Wagner disease 898 Wagner disease is a rare hereditary… Orphanet, MedDRA, MeSH, ICD-10, OMIM
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