Items without sitelinks

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Showing below up to 50 results in range #11,051 to #11,100.

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  1. Chondromalacia, humerus (Q101759)
  2. Chondromalacia, carpus (Q101758)
  3. Chondromalacia, fingers (Q101757)
  4. Chondromalacia, clavicle (Q101756)
  5. 8572/3 (Q101755)
  6. 8560/0 (Q101754)
  7. 8575/3 (Q101753)
  8. Faisalabad histiocytosis (Q101752)
  9. Osteopathy in certain diseases classified elsewhere (Q101751)
  10. Sea-blue histiocytosis (Q101750)
  11. 8562/3 (Q101749)
  12. 8561/0 (Q101748)
  13. 8573/3 (Q101747)
  14. 8560/3 (Q101746)
  15. Stricture of ureteropelvic junction with hydronephrosis and infection (Q101745)
  16. Sinus histiocytosis with massive lymphadenopathy (Q101744)
  17. 8571/3 (Q101743)
  18. Atypical Rett syndrome (Q101742)
  19. Sandhoff disease (Q101741)
  20. 8570/3 (Q101740)
  21. Ring chromosome 20 with normal number of chromosomes (Q101739)
  22. SYNGAP1 syndrome (Q101738)
  23. Autosomal dominant popliteal pterygium syndrome (Q101737)
  24. Bone disorders associated with infection (Q101736)
  25. Infantile perianal warts (Q101735)
  26. 8574/3 (Q101734)
  27. Hypoglossia - hypodactyly (Q101733)
  28. FRAXE intellectual deficit (Q101732)
  29. X-linked cerebral adrenoleukodystrophy (Q101731)
  30. X-linked intellectual deficit, Najm type (Q101730)
  31. Cardioencephalopathy with hyperammonaemia (Q101729)
  32. PEHO syndrome (Q101728)
  33. Distal 17q deletion (Q101727)
  34. Hereditary hyperekplexia (Q101726)
  35. Demyelinating hereditary motor and sensory neuropathy, X-linked (Q101725)
  36. Noonan-like syndrome with loose anagen hair (Q101724)
  37. Infantile bilateral striatal necrosis (Q101723)
  38. X-linked intellectual deficit with isolated growth hormone deficiency (Q101722)
  39. Zellweger-like syndrome without peroxisomal anomalies (Q101721)
  40. Axonal hereditary motor and sensory neuropathy, X-linked (Q101720)
  41. ATR-X-related syndromes (Q101719)
  42. Renpenning syndrome (Q101718)
  43. L1 syndrome (Q101717)
  44. Laurence-Moon syndrome (Q101716)
  45. 8p11.2 deletion (Q101715)
  46. Flexion deformity, toes (Q101714)
  47. Autosomal recessive non-syndromic intellectual deficit (Q101713)
  48. Autosomal dominant non-syndromic intellectual deficit (Q101712)
  49. Greenstick fracture of shaft of tibia (Q101711)
  50. 15q13.3 deletion (Q101710)

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