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6. Contributors

13. Central Type of Neurofibromatosis

14. Cardiomyopathies

15. Cavernous Haemangioma

16. Cardiac Infarction

17. Cardiomyopathy, Dilated

18. Cori-Forbes Disease

19. Cholesterol Ester Hydrolase Deficiency

20. Congenital Myofibromatosis

21. Isolated FSH Deficiency

22. Cerebral Cavernous Angioma

23. Congenital Chloridorrhea

24. Insulin Producing Tumor

25. Congenital Asplenia

26. Chicken Breast

27. Inclusion Body Myopathy, Hereditary

28. Chronic Obstructive Lung Disease

29. Colonic Diverticular Disease

30. Combined Deficiency of Sulfite Oxidase and Xanthine Dehydrogenase

31. CD221 Antigen Defect

32. Congestive Cardiac Failure

33. Copper Excess

34. Chronic Lymphocytic Leukemia

35. Chronic Viral Hepatitis

36. Choroidal Sclerosis

37. Congenital Sucrase-Isomaltase Deficiency

38. Cachexia-Anorexia Syndrome

39. IHES

40. Intercellular IgA Dermatosis

41. Chromosome 13q14 Mutations

42. Idiopathic Neuromyotonia

43. Incontinentia Pigmenti

44. Intestinal Lipodystrophy

45. Congenital Dermal Melanocytosis

46. Congenital Nonautoimmune Hyperthyroidism

47. Iodine Deficiency and Excess

48. Crouzon Craniofacial Dysostosis

49. Cortical Tremor

50. Canavan’s Disease: Aspartoacylase Defect

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