Medicine & Life Sciences

1. Mutation 100%
2. Medium chain acyl CoA dehydrogenase deficiency 92%
3. Metabolic Diseases 74%
4. Hypermanganesemia with Dystonia Polycythemia and Cirrhosis 67%
5. Genes 53%
6. Pediatrics 46%
7. Canada 43%
8. Neonatal Screening 43%
9. Child 42%
10. Neuronal Ceroid-Lipofuscinoses 42%
11. Intellectual Disability 42%
12. Fabry Disease 40%
13. Phenotype 39%
14. Phenylketonurias 38%
15. Thoracic Diseases 37%
16. Aortic Diseases 36%
17. Fibroblasts 35%
18. Chromosome 16p13.3 Deletion Syndrome 35%
19. Manganese 35%
20. Germ-Line Mutation 33%
21. Dissecting Aneurysm 33%
22. Seizures 33%
23. Alagille Syndrome 32%
24. Thoracic Aortic Aneurysm 32%
25. Carnitine palmitoyl transferase 2 deficiency 30%
26. lamin C 26%
27. X-linked sideroblastic anemia 26%
28. Wiskott-Aldrich Syndrome Protein Family 25%
29. Nonketotic Hyperglycinemia 24%
30. Progressive familial intrahepatic 1 Cholestasis 24%
31. Exosome Multienzyme Ribonuclease Complex 24%
32. Iduronidase 24%
33. Tetrasomy 24%
34. Sideroblastic Anemia 23%
35. Ectodermal Dysplasia 23%
36. Acyl-CoA Dehydrogenase 23%
37. Nephrogenic Diabetes Insipidus 22%
38. Isochromosomes 22%
39. Delivery of Health Care 22%
40. Lamins 21%
41. p21-Activated Kinases 21%
42. Benzoates 21%
43. Mucopolysaccharidosis I 21%
44. Dextromethorphan 20%
45. acylcarnitine 20%
46. X Chromosome 20%
47. Lamin Type A 20%
48. GATA2 Deficiency 20%
49. Chromosomes, Human, Pair 19 20%
50. Tandem Mass Spectrometry 20%