Diseases entities [W-X]
Entities range: W-X
Entities count: 103
Entity ID | Entity name |
---|---|
1688996 | WAGR syndrome |
1688475 | WHIM syndrome |
1691345 | WNT4 deficiency |
1689643 | Waardenburg syndrome type 1 |
1691317 | Waardenburg syndrome type 2D |
1691318 | Waardenburg syndrome type 4A |
1688422 | Waardenburg's syndrome |
1689355 | Wagner's disease |
1688926 | Waldenström macroglobulinemia |
1690974 | Waldmann disease |
1688812 | Walker–Warburg syndrome |
1690975 | Wallis–Zieff–Goldblatt syndrome |
1690537 | Warburg micro syndrome |
1689376 | Warfarin Embryopathy |
1711006 | Warfarin resistance |
1710990 | Warsaw breakage syndrome |
1690977 | Warty dyskeratoma |
1687878 | Waterhouse-Friderichsen syndrome |
1688357 | Watson syndrome |
1698861 | Weaver syndrome |
1689791 | Weill-Marchesani syndrome |
1711040 | Weismann-Netter-Stuhl syndrome |
1689382 | Weissenbacher-Zweymuller syndrome |
1688427 | Werner syndrome |
1688773 | Wernicke encephalopathy |
1688283 | West syndrome |
1690978 | Westerhof syndrome |
1691444 | Weyers ulnar ray/oligodactyly syndrome |
1687875 | Whipple disease |
1691360 | White-Sutton syndrome |
1691347 | Wieacker syndrome |
1689649 | Wiedemann-Rautenstrauch syndrome |
1711000 | Wiedemann-Steiner syndrome |
1690979 | Wildervanck syndrome |
1687742 | Williams-Beuren syndrome |
1690980 | Williams-Campbell syndrome |
1687307 | Wilson disease |
1690981 | Wilson–Turner syndrome |
1699162 | Winchester syndrome |
1866413 | Winter's formula |
1688223 | Wiskott-Aldrich syndrome |
1690982 | Wissler's syndrome |
1691218 | Witkop-Von Sallmann disease |
1690983 | Wolcott-Rallison syndrome |
1687806 | Wolf-Hirschhorn syndrome |
1688172 | Wolff–Parkinson–White syndrome |
1688424 | Wolfram syndrome |
1691463 | Wolfram-like syndrome |
1690497 | Wolman disease |
1690984 | Woodhouse–Sakati syndrome |
1690985 | Woolly hair nevus |
1690986 | Worster-Drought syndrome |
1690987 | Worth's syndrome |
1711022 | X linked thrombocytopenia |
1689571 | X-linked adrenal hypoplasia congenita |
1689149 | X-linked adrenoleukodystrophy |
1699163 | X-linked complicated corpus callosum dysgenesis |
1691320 | X-linked cone-rod dystrophy 1 |
1689528 | X-linked dystonia-parkinsonism |
1689801 | X-linked endothelial corneal dystrophy |
1689620 | X-linked hyper IgM syndrome |
1690989 | X-linked hypertrichosis |
1688930 | X-linked hypophosphatemic rickets |
1689747 | X-linked ichthyosis |
1690990 | X-linked intellectual disability |
1691424 | X-linked intellectual disability, Stocco dos Santos type |
1691427 | X-linked intellectual disability-seizures-psoriasis syndrome |
1689618 | X-linked lymphoproliferative disease |
1698827 | X-linked myopathy with excessive autophagy |
1698793 | X-linked myotubular myopathy |
1711032 | X-linked recessive hypoparathyroidism |
1689713 | X-linked reticulate pigmentary disorder |
1689324 | X-linked sideroblastic anemia with ataxia |
1690991 | X-linked spinal muscular atrophy type 2 |
1691328 | XK aprosencephaly |
1699050 | XMEN Disease |
1689147 | XX male syndrome |
1690992 | XXXY syndrome |
1690993 | XXYY syndrome |
1688228 | XY gonadal dysgenesis |
1687557 | XYY syndrome |
1699169 | XYYY syndrome |
1711024 | Xia-Gibbs Syndrome |
1866448 | waist-hip ratio |
1866476 | waist-to-height ratio |
1690976 | warm autoimmune hemolytic anemia |
1866914 | watchful waiting |
1866836 | water deprivation test |
1866979 | wedge resection |
1698879 | wheat allergy |
1689776 | white piedra |
1866953 | whole bowel irrigation |
1710992 | wild-type transthyretin amyloid |
1867106 | withdrawal symptom |
1699160 | woolly hair |
1711049 | wormian bone-multiple fractures-dentinogenesis imperfecta-skeletal dysplasia |
1690988 | wrinkly skin syndrome |
1866955 | wrist arthroscopy |
1690150 | writing disorder |
1688685 | xanthinuria |
1690995 | xanthoma disseminatum |
1687813 | xeroderma pigmentosum |
1688304 | xerophthalmia |