|
Myoclonic Epilepsy and Ragged Red Fibres (MERRF) |
approved
|
545000 |
|
|
|
|
Myoclonic Epilepsy of Unverricht-Lundborg Disease (ULD-EPM1) |
approved
|
254800 |
|
|
|
|
Myoclonus Dystonia (DYT11) |
approved
|
159900 |
|
|
|
|
Myopathy, Myofibrillar 1 |
approved
|
601419 |
|
|
Myopathy, Myofibrillar 10 |
approved
|
619040 |
|
|
|
|
Myopathy, Myofibrillar 2 |
approved
|
608810 |
|
|
|
|
Myopathy, Myofibrillar 3 |
approved
|
609200 |
|
|
|
|
Myopathy, Myofibrillar 4 |
approved
|
609452 |
|
|
|
|
Myopathy, Myofibrillar 5 |
approved
|
609524 |
|
|
|
|
Myopathy, Myofibrillar 6 |
approved
|
612954 |
|
|
|
|
Myopathy, Myofibrillar 7 |
approved
|
617114 |
|
|
|
|
Myopathy, Myofibrillar 8 |
approved
|
617258 |
|
|
|
|
Myopathy, Myofibrillar 9 with early respiratory failure |
approved
|
603689 |
|
|
|
|
Myopathy, Myofibrillar, fatal infantile hypertonic, alpha-B crystallin-related |
approved
|
613869 |
|
|
|
|
Myopathy, spheroid body, (due to mutations in the same gene as myopathy, myofibrillar 3 and with similar phenotype) |
approved
|
182920 |
|
|
|
|
Myotonia Congenita, Autosomal Dominant |
approved
|
160800 |
|
|
|
|
Myotonia Congenita, Autosomal Recessive |
approved
|
255700 |
|
|
|
|
Myotonic Dystrophy |
approved
|
160900 |
|
|
Myotonic Dystrophy type 2 |
approved
|
602668 |
|
|
|
|
Myotubular myopathy |
approved
|
310400, 300219 |
|
