|
Multiple Endocrine Neoplasia type 2B (MEN 2B) |
approved
|
162300 |
|
|
|
|
Multiple Endocrine Neoplasia Type I (MEN1) |
approved
|
131100 |
|
|
Multiple Epiphyseal Dysplasia Type 5 (MED5) |
approved
|
607078 |
|
|
|
|
Multiple Exostoses Type 1 |
approved
|
133700 |
|
|
|
|
Multiple Joint Dislocations, Short Stature and Craniofacial Dysmorphism with or without Congenital Heart Defects (JDSCD) |
approved
|
245600 |
|
|
|
|
Multiple Lentigines Syndrome (LEOPARD Syndrome) |
approved
|
151100 |
|
|
|
|
Multiple Pterygium Syndrome, Escobar variant, EVMPS |
approved
|
265000 |
|
|
|
|
Multiple Sulfatase Deficiency (MSD) |
approved
|
272200 |
|
|
|
|
Muscular Dystrophy (Becker) (BMD) |
approved
|
300376 |
|
|
Muscular Dystrophy (Duchenne)(DMD) |
approved
|
310200 |
|
|
Muscular Dystrophy (Oculopharangeal)(OPMD) |
approved
|
164300 |
|
|
Muscular dystrophy, congenital, Davignon-Chauveau type |
approved
|
617066 |
|
|
|
|
Muscular dystrophy, congenital, due to Integrin alpha-7 deficiency |
approved
|
613204 |
|
|
|
|
Muscular Dystrophy, Congenital, LMNA-related, (MDCL) - for cases where there is proven evidence of mosaicism in the blood or as a result of a second affected child |
approved
|
613205 |
|
|
|
|
Muscular dystrophy, congenital, megaconial type |
approved
|
602541 |
|
|
|
|
Muscular dystrophy, congenital, with cataracts and intellectual disability |
approved
|
617404 |
|
|
|
|
Muscular dystrophy, Limb-Girdle (LGMD) Type 1B |
approved
|
159001 |
|
|
|
|
Muscular dystrophy, limb-girdle, autosomal recessive 17 |
approved
|
613723 |
|
|
|
|
Muscular dystrophy, limb-girdle, type 2C |
approved
|
253700 |
|
|
|
|
Muscular dystrophy, limb-girdle, type 2S |
approved
|
615356 |
|
|
|
