Items without sitelinks

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Showing below up to 50 results in range #9,101 to #9,150.

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  1. Acute gallbladder abscess (Q103709)
  2. Unintentional exposure to or harmful effects of mercury or its compounds (Q103708)
  3. Unintentional exposure to or harmful effects of dishwasher detergent (Q103707)
  4. Unintentional exposure to or harmful effects of tin or its compounds (Q103706)
  5. Unintentional exposure to or harmful effects of toothpaste (Q103705)
  6. Meadow dermatitis (Q103704)
  7. Unintentional exposure to or harmful effects of thallium (Q103703)
  8. Unintentional exposure to or harmful effects of soaps (Q103702)
  9. Strimmer dermatitis (Q103701)
  10. Sporotrichosis arthritis (Q103700)
  11. Unintentional exposure to or harmful effects of beryllium or its compounds (Q103699)
  12. Unintentional exposure to or harmful effects of nitrogen oxides (Q103698)
  13. Unintentional exposure to or harmful effects of cadmium or its compounds (Q103697)
  14. Unintentional exposure to or harmful effects of zinc or its compounds (Q103696)
  15. Acute emphysematous cholecystitis without calculus (Q103695)
  16. Congenital muscular dystrophy, Paradas type (Q103694)
  17. Congenital muscular dystrophy with integrin deficiency (Q103693)
  18. Congenital muscular dystrophy type 1C, fukutin-related protein gene mutation (Q103692)
  19. Congenital muscular dystrophy with central nervous system abnormalities, not elsewhere classified (Q103691)
  20. Phototoxic reaction to topical psoralen therapy (Q103690)
  21. Congenital muscular dystrophy type 1D large gene mutation (Q103689)
  22. Occupational phototoxic reaction to skin contact with plant matter (Q103688)
  23. Suxamethonium paralysis (Q103687)
  24. Congenital muscular dystrophy type 1B (Q103686)
  25. Hogweed dermatitis (Q103685)
  26. Analbuminaemia (Q103684)
  27. Congenital atransferrinaemia (Q103683)
  28. Bisalbuminaemia (Q103682)
  29. Hyperproteinaemia (Q103681)
  30. Hypoalbuminemia (Q103680)
  31. Marinesco-Sjögren syndrome (Q103679)
  32. Para-albuminemia (Q103678)
  33. Deficiency of cholinesterase (Q103677)
  34. Rigid spine syndrome (Q103676)
  35. Inversion of albumin-globulin ratio (Q103675)
  36. Absence of albumin in blood (Q103674)
  37. Congenital muscular dystrophy without central nervous system abnormalities, not elsewhere classified (Q103673)
  38. Congenital muscular dystrophy due to phosphatidylcholine biosynthesis defect (Q103672)
  39. Congenital muscular dystrophy - infantile cataract - hypogonadism (Q103671)
  40. O-fucose-specific beta-1,3-N-acetylglucosaminyltransferase deficiency (Q103670)
  41. O-fucose-specific beta-1,3-N-glucosyltransferase deficiency (Q103669)
  42. Component of conserved oligomeric Golgi complex 5 deficiency (Q103668)
  43. Congenital muscular dystrophy due to lamin A/C deficiency (Q103667)
  44. Component of conserved oligomeric Golgi complex 4 deficiency (Q103666)
  45. Typical aura without headache (Q103665)
  46. Typical aura with headache (Q103664)
  47. Collagen VI deficiency (Q103663)
  48. N-acetylglucosaminyltransferase-like protein deficiency (Q103662)
  49. Component of conserved oligomeric Golgi complex 7 deficiency (Q103661)
  50. Component of conserved oligomeric Golgi complex 8 deficiency (Q103660)

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