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Wikipedia:WikiProject Missing encyclopedic articles/Missing diseases/11

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WikiProject Missing encyclopedic articles
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  1. Ulna metaphyseal dysplasia syndrome
  2. Unna-Politzer nevus
  3. Upper limb defect eye and ear abnormalities
  4. Urethral obstruction sequence
  5. Urophathy distal obstructive polydactyly
  6. VACTERL association with hydrocephaly, X linked
  7. VACTERL hydrocephaly
  8. Vagneur Triolle Ripert syndrome
  9. Van Allen Myhre syndrome
  10. Van Bogaert-Hozay syndrome
  11. Van Regemorter Pierquin Vamos syndrome
  12. Vascular disruption sequence
  13. Vascular helix of umbilical cord
  14. Vascular malposition
  15. Velofacioskeletal syndrome
  16. Verloes Bourguignon syndrome
  17. Verloes David syndrome
  18. Verloes Gillerot Fryns syndrome
  19. Verloove Vanhorick Brubakk syndrome
  20. Verrucous nevus acanthokeratolytic
  21. Verrucous nevus
  22. Vestibular paroxysmia
  23. Vertebral body fusion overgrowth
  24. Vertebral fusion posterior lumbosacral blepharoptosis
  25. Viljoen Winship syndrome
  26. Virilizing ovarian tumor
  27. Virus associated hemophagocytic syndrome
  28. Vitiligo mental retardation facial dysmorphism uremia
  29. Vitiligo psychomotor retardation cleft palate facial dysmorphism
  30. Vitreoretinal degeneration
  31. W syndrome
  32. Waaler Aarskog syndrome
  33. Walbaum Titran Durieux Crepin syndrome
  34. Walker Dyson syndrome
  35. Warburton Anyane Yeboa syndrome
  36. Weaver Johnson syndrome
  37. Weaver Williams syndrome
  38. Webster Deming syndrome
  39. Wegmann Jones Smith syndrome
  40. Weinstein Kliman Scully syndrome
  41. Weleber Hecht Bigley syndrome
  42. Wellesley Carmen French syndrome
  43. Whyte Murphy syndrome
  44. Wiedemann Oldigs Oppermann syndrome
  45. Winkelman Bethge Pfeiffer syndrome
  46. Winship Viljoen Leary syndrome
  47. Winter Harding Hyde syndrome
  48. Wisconsin syndrome
  49. Woods Black Norbury syndrome
  50. Woods Leversha Rogers syndrome
  51. Wright Dick syndrome
  52. Wt limb blood syndrome
  53. X chromosome, duplication Xq13 1 q21 1
  54. X chromosome, monosomy Xp22 pter
  55. X chromosome, monosomy Xq28
  56. X chromosome, trisomy Xp3
  57. X chromosome, trisomy Xpter Xq13
  58. X chromosome, trisomy Xq
  59. X chromosome, trisomy Xq25
  60. X fragile site folic acid type
  61. Xerocytosis, hereditary
  62. Xeroderma talipes enamel defects
  63. Yorifuji Okuno syndrome
  64. Yoshimura-Takeshita syndrome
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