Wikipedia:WikiProject Missing encyclopedic articles/Missing diseases/11

<< Previous · ^up^ · Next >>

---

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