Items without sitelinks

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Showing below up to 50 results in range #7,501 to #7,550.

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  1. 8144/3 (Q105309)
  2. Malignant neoplasm metastasis in lower gingiva (Q105308)
  3. Malignant neoplasm metastasis in tonsillar region (Q105307)
  4. Malignant neoplasm metastasis in upper gingiva (Q105306)
  5. Malignant neoplasm metastasis in retromolar area (Q105305)
  6. 8141/3 (Q105304)
  7. Nutritional dystrophy (Q105303)
  8. Ring chromosome 12 with normal number of chromosomes (Q105302)
  9. Certain specified nutritional deficiencies (Q105301)
  10. Undernutrition based on anthropometric or clinical criteria in infants, children or adolescents (Q105300)
  11. Ring chromosome 22 with normal number of chromosomes (Q105299)
  12. Ring chromosome 21 with normal number of chromosomes (Q105298)
  13. Ring chromosome 17 with normal number of chromosomes (Q105297)
  14. Vitamin deficiencies (Q105296)
  15. Ring chromosome 18 with normal number of chromosomes (Q105295)
  16. Undernutrition based on anthropometric or clinical criteria in adults (Q105294)
  17. Ring chromosome 13 with normal number of chromosomes (Q105293)
  18. Ring chromosome 19 with normal number of chromosomes (Q105292)
  19. Mechanical complication of intrauterine contraceptive device (Q105291)
  20. Ring chromosome 16 with normal number of chromosomes (Q105290)
  21. Ring chromosome 15 with normal number of chromosomes (Q105289)
  22. Ring chromosome 14 with normal number of chromosomes (Q105288)
  23. Central polydactyly of fingers, unilateral (Q105287)
  24. D-2-hydroxyglutaric aciduria (Q105286)
  25. Ring chromosome 4 with normal number of chromosomes (Q105285)
  26. Ring chromosome 5 with normal number of chromosomes (Q105284)
  27. Ring chromosome 6 with normal number of chromosomes (Q105283)
  28. Kidney transplant associated with injury or harm, open approach (Q105282)
  29. Ring chromosome 7 with normal number of chromosomes (Q105281)
  30. Ring chromosome 10 with normal number of chromosomes (Q105280)
  31. Ring chromosome 3 with normal number of chromosomes (Q105279)
  32. Ring chromosome 11 with normal number of chromosomes (Q105278)
  33. WHIM - [Warts-hypogammaglobulinaemia-infections-myelokathexis] syndrome (Q105277)
  34. L-2-hydroxyglutaric aciduria (Q105276)
  35. Unbalanced reciprocal translocation with 2:2 segregation (chromosome count = 46) (Q105275)
  36. Majeed syndrome (Q105274)
  37. Ring chromosome 8 with normal number of chromosomes (Q105273)
  38. Polydactyly of an index finger (Q105272)
  39. Central polydactyly of fingers, bilateral (Q105271)
  40. Ring chromosome 2 with normal number of chromosomes (Q105270)
  41. Unbalanced reciprocal translocation with 3:1 segregation (chromosome count = 45) (Q105269)
  42. Ring chromosome 9 with normal number of chromosomes (Q105268)
  43. Subacute spongiform encephalopathy (Q105267)
  44. Unbalanced reciprocal translocation with 3:1 segregation (chromosome count = 47) (Q105266)
  45. 9725/3 (Q105265)
  46. Ring chromosome 1 with normal number of chromosomes (Q105264)
  47. Neurological conditions associated with aminoacylase 1 deficiency (Q105263)
  48. Autoinflammatory disease due to interleukin-1 receptor antagonist deficiency (Q105262)
  49. Multiple pterygium syndrome, X-linked (Q105261)
  50. Incessant infant ventricular tachycardia (Q105260)

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