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Showing below up to 50 results in range #8,501 to #8,550.

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  1. Internal granuloma of pulp (Q104309)
  2. Familial pulmonary arterial hypertension due to BMPR2 mutations (Q104308)
  3. Pulmonary arterial hypertension associated with congenital heart disease (Q104307)
  4. Certain specified disorders of the visual organs (Q104306)
  5. Pulmonary capillary haemangiomatosis (Q104305)
  6. Juvenile systemic arthritis, fingers (Q104304)
  7. Pulmonary arterial hypertension associated with connective tissue diseases (Q104303)
  8. Juvenile systemic arthritis, elbow joint (Q104302)
  9. Juvenile systemic arthritis, carpus (Q104301)
  10. Pulmonary arterial hypertension associated with HIV infection (Q104300)
  11. Familial pulmonary arterial hypertension due to ALK1 or endoglin mutations (Q104299)
  12. Pulmonary arterial hypertension associated with portal hypertension (Q104298)
  13. Juvenile systemic arthritis, glenohumeral joint (Q104297)
  14. Juvenile systemic arthritis, acromioclavicular joint (Q104296)
  15. Familial pulmonary arterial hypertension of unknown origin (Q104295)
  16. Methylmalonyl-CoA epimerase deficiency (Q104294)
  17. Liver transplant failure (Q104293)
  18. Extent or magnitude of impairment (Q104292)
  19. Complete deficiency of methylmalonyl-CoA mutase (Q104291)
  20. Anatomical localization (Q104290)
  21. Performance (Q104289)
  22. Barrier or facilitator (Q104288)
  23. Capacity (Q104287)
  24. Heart-lung transplant rejection (Q104286)
  25. Nature of change in body structure (Q104285)
  26. Environmental factors (Q104284)
  27. Methylmalonyl-CoA epimerase deficiency with sepiapterin reductase deficiency (Q104283)
  28. Partial deficiency of methylmalonyl-CoA mutase (Q104282)
  29. Functioning Situation (Q104281)
  30. Heart-lung transplant failure (Q104280)
  31. Body functions (Q104279)
  32. Occupational non-allergic contact urticaria (Q104278)
  33. Liver transplant rejection (Q104277)
  34. Environmental Factor Role (Q104276)
  35. Body structures (Q104275)
  36. Activities and participation (Q104274)
  37. Autosomal dominant Charcot-Marie-Tooth disease type 2O (Q104273)
  38. Autosomal recessive Charcot-Marie-Tooth disease with hoarseness (Q104272)
  39. Recessive axonal Charcot-Marie-Tooth disease with acrodystrophy (Q104271)
  40. Charcot-Marie-Tooth disease type 2C (Q104270)
  41. Charcot-Marie-Tooth disease type 2E (Q104269)
  42. Charcot-Marie-Tooth disease type 2H (Q104268)
  43. Charcot-Marie-Tooth disease type 2G (Q104267)
  44. Autosomal dominant Charcot-Marie-Tooth disease type 2N (Q104266)
  45. Autosomal dominant Charcot-Marie-Tooth disease type 2M (Q104265)
  46. Charcot-Marie-Tooth disease type 2D (Q104264)
  47. Charcot-Marie-Tooth disease type 2B2 (Q104263)
  48. Charcot-Marie-Tooth disease type 2I (Q104262)
  49. Charcot-Marie-Tooth disease type 2J (Q104261)
  50. Charcot-Marie-Tooth disease type 2K (Q104260)

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