molecular biology digital assignment topics

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Here are 68 diseases caused by multiple DNA repair mechanism malfunctions:

1. Xeroderma Pigmentosum (XP)

2. Ataxia-Telangiectasia (A-T)

3. Bloom Syndrome (BS)

4. Fanconi Anemia (FA)

5. Cockayne Syndrome (CS)

6. Werner Syndrome (WS)

7.Nijmegen Breakage Syndrome (NBS)

8. Hereditary Breast and Ovarian Cancer Syndrome (HBOC)

9. DNA Repair-Deficiency Syndrome (RIDDLE Syndrome)

10. Nucleotide Excision Repair Deficiency Syndrome (NERDS)

11. Seckel Syndrome

12. PIBIDS Syndrome

13. Trichothiodystrophy

14. RAPADILINO Syndrome

15. Rothmund-Thomson Syndrome

16 . Li-Fraumeni Syndrome

17. Retinoblastoma

18. Neurofibromatosis Type 1

19. Neurofibromatosis Type 2

20. Basal Cell Nevus Syndrome (Gorlin Syndrome)

21. Bloom-Torre-Machacek Syndrome

22. Atypical Xeroderma Pigmentosum Syndrome

23. UV-sensitive Syndrome

24. Spinocerebellar Ataxia with Axonal

 25.Neuropathy Type 1

26. Autosomal Recessive Ataxia of Charlevoix-Saguenay

27. Microcephaly with or without Chorioretinopathy, Lymphedema, or Mental Retardation

28. Aicardi-Goutières Syndrome

29. Cerebro-oculo-facio-skeletal Syndrome

30. Nance-Horan Syndrome

31. Marden-Walker Syndrome

32. Pfeiffer Syndrome

33. Apert Syndrome

34. Saethre-Chotzen Syndrome

35. Craniosynostosis with Ocular Abnormalities and Hallucal Defects
Baller-Gerold Syndrome

36. Short Stature, Optic Nerve Atrophy, and Pelger-Huët Anomaly

37. Cockayne Syndrome Type 2

38. Atypical Werner Syndrome

39. XP Variant

40. Hereditary Nonpolyposis Colorectal Cancer (Lynch Syndrome)

41. Familial Adenomatous Polyposis

42. Peutz-Jeghers Syndrome

43. Cowden Syndrome

44. Constitutional Mismatch Repair Deficiency Syndrome

45. MUTYH-Associated Polyposis

46. DNA Polymerase Epsilon Deficiency

47. DNA Ligase I Deficiency

48. Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome

49. Schimke Immunoosseous Dysplasia

50. Cockayne Syndrome Type 3

51. Nijmegen Breakage Syndrome-Like Disorder

52. Severe Combined Immunodeficiency

53. Ataxia-Oculomotor Apraxia Type 1

54. Ataxia-Oculomotor Apraxia Type 2

55. ATR-16 Syndrome

56. Autosomal Dominant Cerebellar Ataxia

57. Autosomal Recessive Cerebellar Ataxia

58. Cone-Rod Dystrophy

59. Retinitis Pigmentosa

60. Leber Congenital Amaurosis

61.Neurodegeneration with Brain Iron Accumulation

62. Frontotemporal Dementia

63. Amyotrophic Lateral Sclerosis

64. Huntington Disease

65. Parkinson Disease

66. Alzheimer Disease

67. Cockayne Syndrome Type 1

68. Trichothiodystrophy with Photos

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