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 |