Diseases

Name Orphanumber Description XREF(s)
Weissenbacher- Zweymuller syndrome 3450 Weissenbacher-Zweymuller syndrome (WZS… Orphanet, ICD-10, OMIM
Well-differentiated liposarcoma 99971 Well-differentiated liposarcoma (WDLS… Orphanet, ICD-10
Werner syndrome 902 Werner syndrome (WS) is a rare… Orphanet, MeSH, MedDRA, OMIM, ICD-10
WHIM syndrome 51636 WHIM (warts, hypogammaglobulinemia,… Orphanet, MeSH, OMIM, ICD-10
Whipple disease 3452 A rare chronic infectious disorder in… Orphanet, ICD-10, MeSH, MeSH, MedDRA, ICD-10
White sponge nevus 171723 White sponge nevus (WSN) is a rare and… Orphanet, ICD-10, OMIM, OMIM
White-Sutton syndrome 468678 A rare, genetic, syndromic intellectual… Orphanet, ICD-10, OMIM
Wiedemann-Rautenstrauch syndrome 3455 A rare multiple congenital anomalies/… Orphanet, MeSH, OMIM, ICD-10
Wiedemann-Steiner syndrome 319182 A rare, genetic multiple congenital… Orphanet, ICD-10, OMIM
Williams syndrome 904 A rare genetic multisystemic… Orphanet, ICD-10, MedDRA, OMIM, MeSH
Wilson disease 905 A rare genetic disorder of copper… Orphanet, MeSH, MedDRA, ICD-10, OMIM
Wilson-Turner syndrome 3459 Wilson-Turner syndrome (WTS) is a very… Orphanet, ICD-10, OMIM
Wiskott-Aldrich syndrome 906 A primary immunodeficiency disease… Orphanet, MeSH, MedDRA, ICD-10, OMIM, OMIM, OMIM
Wolcott-Rallison syndrome 1667 Wolcott-Rallison syndrome (WRS) is a… Orphanet, OMIM, MeSH, ICD-10
Wolf-Hirschhorn syndrome 280 A developmental disorder characterized… Orphanet, MeSH, MeSH, OMIM, MedDRA, ICD-10
Wolfram syndrome 3463 A rare, genetic, endocrine disorder… Orphanet, ICD-10, MeSH, OMIM, OMIM, OMIM
Wolfram-like syndrome 411590 Wolfram-like syndrome is a rare… Orphanet, ICD-10, OMIM
Wolman disease 75233 A severe form of lysosomal acid lipase… Orphanet, OMIM, MeSH, MedDRA, ICD-10
Woodhouse-Sakati syndrome 3464 Woodhouse-Sakati syndrome is a… Orphanet, ICD-10, MeSH, OMIM
Woolly hair 170 A rare congenital skin disease defined… Orphanet, MeSH, ICD-10, OMIM, OMIM, OMIM, OMIM, OMIM, MedDRA
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