113. Muscular dystrophy Clinical trials / Disease details
Clinical trials : 646 / Drugs : 471 - (DrugBank : 105) / Drug target genes : 59 - Drug target pathways : 170
Previous names | - | ||
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Other names | - | ||
Disease group | Neuromuscular diseases | ||
Related info (in Japanese) | |||
Specific pediatric chronic diseases, Japan (in Japanese) | 11-20-52. Muscular dystrophy | ||
Subtypes | No. | Name | Specific pediatric chronic diseases, Japan (in Japanese) |
113-1. | Dystrophinopathies; | ||
113-2. | Duchenne muscular dystrophy;DMD; | 11-20-45. Duchenne muscular dystrophy | |
113-3. | Becker muscular dystrophy; | 11-20-52. Muscular dystrophy | |
113-4. | Limb-girdle muscular dystrophy; | 11-20-47. limb-girdle muscular dystrophy | |
113-5. | Myotilinopathy; | ||
113-6. | Laminopathy; | ||
113-7. | Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C; | ||
113-8. | Desminopathy; | ||
113-9. | Sarcoglycanopathy; | ||
113-10. | α-dystroglycanopathy; | ||
113-11. | Congenital muscular dystrophy; | ||
113-12. | Facioscapulohumeral muscular dystrophy; | 11-20-48. facio-scapulohumeral muscular dystrophy; FSMD | |
113-13. | Emery-Dreifuss muscular dystrophy; | 11-20-46. Emery-Dreifuss muscular dystrophy | |
113-14. | Oculopharyngeal muscular dystrophy; | ||
113-15. | Fukuyama-type congenital muscular dystrophy;FCMD; | 11-20-49. Fukuyama congenital muscular dystrophy; FCMD | |
113-16. | Walker-Warburg syndrome; | ||
113-17. | Muscle-eye-brain disease; | ||
113-18. | Myotonic dystrophy; | 11-20-52. Muscular dystrophy | |
113-19. | Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy; | ||
113-20. | Merosin-deficient congenital muscular dystrophy; | 11-20-50. merosin-deficient congenital muscular dystrophy | |
113-21. | Ullrich congenital muscular dystrophy; | 11-20-52. Muscular dystrophy | |
113-22. | Rigid spine syndrome; | ||
113-23. | Dynamin 2 deficient congenital muscular dystrophy; | ||
113-24. | Telesonin-deficient congenital muscular dystrophy; | ||
113-25. | Congenital muscular dystrophy with mitochondrial structural abnormalities; |