Items without sitelinks

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Showing below up to 50 results in range #24,001 to #24,050.

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  1. Relaxation of diaphragm (Q88809)
  2. Monstrocellular sarcoma of unspecified site (Q88808)
  3. Puerperal lymphangitis (Q88807)
  4. Baghdad spring anaemia (Q88806)
  5. Renal glycosuria associated with familial or genetic disorders elsewhere classified (Q88805)
  6. Open wound of wrist, unspecified (Q88804)
  7. Puerperal infection, not elsewhere classified (Q88803)
  8. Paralysis of diaphragm (Q88802)
  9. Diaphragmitis (Q88801)
  10. Secondary thrombocytopenic purpura specified as refractory (Q88800)
  11. Acute pelvic pain (Q88799)
  12. Open wound of hand, unspecified (Q88798)
  13. Neuroblastoma of unspecified site (Q88797)
  14. Sagittal fracture of the maxilla (Q88796)
  15. Spondylolisthesis without pars defect with no determinant (Q88795)
  16. Hereditary haemolytic nonspherocytic type 1 anaemia (Q88794)
  17. Spondylolisthesis without pars defect with determinant (Q88793)
  18. Fracture of maxillary sinus (Q88792)
  19. Mesonephromas- ICD-O3 view (Q88791)
  20. Dilutional thrombocytopenia (Q88790)
  21. Fracture of alveolar ridge of maxilla (Q88789)
  22. Renal glycosuria associated with acute or chronic renal failure (Q88788)
  23. Ossification of diaphragm (Q88787)
  24. Acquired diaphragmatic deformity (Q88786)
  25. Holoprosencephaly - craniosynostosis (Q88785)
  26. Trichiasis without entropion lower eyelid (Q88784)
  27. Porcelain gallbladder (Q88783)
  28. Xanthogranulomatous cholecystitis (Q88782)
  29. Distal deletions of the short arm of chromosome 3 (Q88781)
  30. Trichiasis without entropion upper eyelid (Q88780)
  31. Sensations associated with the eye and adjoining structures (Q88779)
  32. Immunobullous dermatosis classified elsewhere precipitated by drug (Q88778)
  33. Late chronic graft-versus-host disease (Q88777)
  34. Early chronic graft-versus-host disease (Q88776)
  35. Functions of structures adjoining the eye (Q88775)
  36. Seeing functions (Q88774)
  37. XK aprosencephaly (Q88773)
  38. Proximal deletions of the short arm of chromosome 3 (Q88772)
  39. Subjective tinnitus (Q88771)
  40. Unclassifiable benign cutaneous melanocytic proliferation (Q88770)
  41. Special types of melanocytic naevus (Q88769)
  42. Spindle cell melanocytic naevus (Q88768)
  43. Claude syndrome (Q88767)
  44. Complete trisomy 13, translocation (Q88766)
  45. Nondiabetic hypoglycaemic coma (Q88765)
  46. Weber syndrome (Q88764)
  47. Complete trisomy 13, meiotic non-disjunction (Q88763)
  48. Polyneuropathy in hypoglycaemia (Q88762)
  49. Congenital dyserythropoietic anaemia type III (Q88761)
  50. Self-damaging behaviour (Q88760)

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