Items without sitelinks

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Showing below up to 50 results in range #4,751 to #4,800.

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  1. nephrology (Q17627)
  2. kidney disease (Q17626)
  3. rare genetic renal disease (Q17625)
  4. nephropathy secondary to a storage or other metabolic disease (Q17624)
  5. propionyl-CoA biosynthetic process (Q17623)
  6. dystonia (Q17622)
  7. dystonic disorders (Q17621)
  8. rare genetic dystonia (Q17620)
  9. rare disorder with dystonia and other neurologic or systemic manifestation (Q17619)
  10. propionyl-CoA catabolic process (Q17618)
  11. neurometabolic disease (Q17617)
  12. propionyl-CoA metabolic process (Q17616)
  13. rare genetic epilepsy (Q17615)
  14. 2-ketobutyrate formate-lyase activity (Q17614)
  15. metabolic diseases with epilepsy (Q17613)
  16. metal transport or utilization disorder with epilepsy (Q17612)
  17. acryloyl-CoA reductase (NADP+) activity (Q17611)
  18. rare metabolic liver disease (Q17610)
  19. 2-oxobutyrate synthase activity (Q17609)
  20. genetic movement disorder (Q17608)
  21. rare genetic tremor disorder (Q17607)
  22. propionyl-CoA:succinate CoA-transferase activity (Q17606)
  23. supranuclear oculomotor palsy (Q17605)
  24. propionyl-CoA C2-trimethyltridecanoyltransferase activity (Q17604)
  25. cornea symptom (Q17603)
  26. 2-methylcitrate synthase activity (Q17602)
  27. fibrous tunic of eyeball (Q17601)
  28. cornea (Q17600)
  29. corneal disease (Q17599)
  30. corneal opacity (Q17598)
  31. metabolic disease with corneal opacity (Q17597)
  32. propionate-CoA ligase activity (Q17596)
  33. hereditary eye disease (Q17595)
  34. rare eye disease (Q17594)
  35. rare genetic eye disease (Q17593)
  36. metabolic disease associated with ocular features (Q17592)
  37. metabolic disease with cataract (Q17591)
  38. rare hereditary metabolic disease with peripheral neuropathy (Q17590)
  39. copper metabolism disease (Q17589)
  40. Wilson disease (Q17588)
  41. metal metabolism disorder (Q17587)
  42. inherited metabolic disorder (Q17586)
  43. overload disease (Q17585)
  44. ironeman (Q17584)
  45. disorder of metabolite absorption and transport (Q17583)
  46. mineral metabolism disease (Q17582)
  47. iron metabolism disease (Q17581)
  48. iron overload (Q17580)
  49. HFE hereditary haemochromatosis (Q17579)
  50. rare genetic gastroenterological disease (Q17578)

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