Medicine & Life Sciences

1. Congenital Disorders of Glycosylation 100%
2. Glycosylation 46%
3. Mutation 28%
4. Phenotype 26%
5. Cutis Laxa 25%
6. Mitochondrial Diseases 21%
7. Intellectual Disability 19%
8. Cutis Laxa, Autosomal Recessive, Type I 18%
9. Genes 16%
10. Child 15%
11. Muscle Hypotonia 15%
12. Polysaccharides 13%
13. Glycogen Storage Disease XIV 13%
14. Transferrin 13%
15. Oxidative Phosphorylation 12%
16. Galactose 12%
17. Fibroblasts 12%
18. Inborn Errors Metabolism 11%
19. 3-Methylglutaconic Aciduria 10%
20. Phosphoglucomutase 9%
21. Neurodevelopmental Disorders 9%
22. Congenital disorder of glycosylation type II 9%
23. Undiagnosed Diseases 9%
24. Exome 8%
25. phosphomannomutase 8%
26. Muscles 8%
27. Microcephaly 8%
28. Seizures 7%
29. Enzymes 7%
30. Congenital disorder of glycosylation type 1A 7%
31. Epilepsy 7%
32. Leigh Disease 7%
33. Brain Diseases 6%
34. Methylmalonic acidemia 6%
35. Ataxia 6%
36. Proteins 6%
37. Muscular Diseases 6%
38. Brain 6%
39. Therapeutics 5%
40. Dolichols 5%
41. Skin 5%
42. Deafness 5%
43. Type In Congenital Disorder of Glycosylation 5%
44. Apolipoprotein C-III 5%