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Showing below up to 50 results in range #15,751 to #15,800.

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  1. Raeder paratrigeminal syndrome (Q97059)
  2. Miescher's elastoma (Q97058)
  3. Gastritis due to Crohn disease (Q97057)
  4. Neuropathies causing ophthalmoplegia (Q97056)
  5. Sialidosis type 2 (Q97055)
  6. Orbital apex syndromes (Q97054)
  7. Gastric mucosal hyperplasia (Q97053)
  8. Alpha-N-acetylgalactosaminidase deficiency type 1 (Q97052)
  9. Hyperplastic gastropathy of mucous cell type (Q97051)
  10. Infantile alpha-mannosidosis (Q97050)
  11. Alpha-N-acetylgalactosaminidase deficiency type 2 (Q97049)
  12. Sialidosis type 1 (Q97048)
  13. Adult alpha-mannosidosis (Q97047)
  14. Gastritis due to vasculitis (Q97046)
  15. Superior orbital fissure syndromes (Q97045)
  16. Familial partial lipodystrophy, Dunnigan type (Q97044)
  17. 9580/3 (Q97043)
  18. Spontaneous rupture of synovium, metacarpus (Q97042)
  19. Parinaud ophthalmoplegia (Q97041)
  20. Necrotising fasciitis, toes (Q97040)
  21. Spontaneous rupture of synovium, carpus (Q97039)
  22. Erythema induratum of Bazin (Q97038)
  23. LAMB syndrome (Q97037)
  24. 9582/0 (Q97036)
  25. External ophthalmoplegia, not elsewhere classified (Q97035)
  26. Familial partial lipodystrophy due to lamin-A mutations (Q97034)
  27. Ocular neuromyotonia (Q97033)
  28. Spontaneous rupture of synovium, fingers (Q97032)
  29. Superior oblique myokymia (Q97031)
  30. Familial partial lipodystrophy, Köbberling type (Q97030)
  31. Familial partial lipodystrophy associated with PPARG mutations (Q97029)
  32. Stress lymphocytosis (Q97028)
  33. 9580/0 (Q97027)
  34. Familial partial lipodystrophy due to AKT2 mutations (Q97026)
  35. Mandibuloacral dysplasia with type A lipodystrophy (Q97025)
  36. Mandibuloacral dysplasia with type B lipodystrophy (Q97024)
  37. 9581/3 (Q97023)
  38. Erythema induratum of Whitfield (Q97022)
  39. Familial partial lipodystrophy associated with PLIN1 mutations (Q97021)
  40. Spontaneous rupture of synovium, ankle joint (Q97020)
  41. Spontaneous rupture of synovium, acromioclavicular joint (Q97019)
  42. ALAD porphyria (Q97018)
  43. Spontaneous rupture of synovium, tarsus (Q97017)
  44. Spontaneous rupture of synovium, toes (Q97016)
  45. Spontaneous rupture of synovium, humerus (Q97015)
  46. Spontaneous rupture of synovium, hip joint (Q97014)
  47. Hereditary coproporphyria (Q97013)
  48. Spontaneous rupture of synovium, wrist joint (Q97012)
  49. Homozygous hereditary coproporphyria (Q97011)
  50. Spontaneous rupture of synovium, sternoclavicular joint (Q97010)

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