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Showing below up to 50 results in range #26,151 to #26,200.

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  1. Primary intra-abdominal hernia with obstruction without gangrene (Q86659)
  2. Tarsometatarsal strain (Q86658)
  3. Exhaustion due to excessive exertion (Q86657)
  4. Certain specified disorders of parathyroid gland (Q86656)
  5. Trigeminal trophic syndrome (Q86655)
  6. Primary intra-abdominal hernia with gangrene (Q86654)
  7. Tarsal sprain (Q86653)
  8. Circulatory collapse following pregnancy with abortive outcome (Q86652)
  9. Midtarsal sprain (Q86651)
  10. Non-alcoholic fatty liver disease associated with metabolic disorders attributable to over-nutrition (Q86650)
  11. Paralysis of combined upgaze and downgaze (Q86649)
  12. Non-alcoholic fatty liver disease, not elsewhere classified (Q86648)
  13. Dorsal midbrain syndrome (Q86647)
  14. Tarsometatarsal sprain (Q86646)
  15. Paralysis of downgaze (Q86645)
  16. Circulatory collapse following molar or ectopic pregnancy (Q86644)
  17. Midtarsal strain (Q86643)
  18. Paralysis of upgaze (Q86642)
  19. Vertical one-and-a-half syndrome (Q86641)
  20. Shock following pregnancy with abortive outcome (Q86640)
  21. Diverticulum of rectosigmoid (Q86639)
  22. Tarsal strain (Q86638)
  23. Hereditary motor or sensory neuropathy, Okinawa type (Q86637)
  24. Diverticulum of caecum (Q86636)
  25. Neuropathic muscular atrophy (Q86635)
  26. Diverticulum of sigmoid (Q86634)
  27. Myelitis due to schistosoma species (Q86633)
  28. Hereditary ataxia-muscular atrophy syndrome (Q86632)
  29. Roussy-Levy syndrome (Q86631)
  30. Myelitis due to Coenurus cerebralis (Q86630)
  31. Charcot-Marie-Tooth type paralysis (Q86629)
  32. Progressive hypertrophic interstitial neuropathy (Q86628)
  33. Hypertrophic hereditary neuropathy (Q86627)
  34. Progressive neuropathic muscular atrophy (Q86626)
  35. Charcot-Marie-Tooth type progressive muscular dystrophy (Q86625)
  36. Axonal peroneal muscular atrophy (Q86624)
  37. Chondromalacia, ankle or foot (Q86623)
  38. Charcot-Marie-Tooth hypertrophic neuropathy (Q86622)
  39. Structural developmental anomalies of sternocleidomastoid muscle (Q86621)
  40. Dejerine-Sottas syndrome (Q86620)
  41. Chondromalacia, vertebral column (Q86619)
  42. Chondromalacia, skull (Q86618)
  43. Chondromalacia, lower leg (Q86617)
  44. Hereditary motor or sensory neuropathy type 5 (Q86616)
  45. Hereditary thermosensitive neuropathy (Q86615)
  46. Lateral fistula of the neck (Q86614)
  47. Intramedullary granuloma due to cysticercosis (Q86613)
  48. Chondromalacia, neck (Q86612)
  49. Acquired abnormality of the right-sided atrioventricular valve in double inlet ventricle (Q86611)
  50. Mucopolysaccharidosis type 4A (Q86610)

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