| C0270962 |
Multi-core congenital myopathy |
DO |
muscular dystrophy-dystroglycanopathy
|
0050588 |
| C0270962 |
Multi-core congenital myopathy |
DO |
megaconial type congenital muscular dystrophy
|
0110632 |
| C0270962 |
Multi-core congenital myopathy |
DO |
rigid spine muscular dystrophy 1
|
0110633 |
| C0270962 |
Multi-core congenital myopathy |
DO |
congenital muscular dystrophy 1B
|
0110634 |
| C0270962 |
Multi-core congenital myopathy |
DO |
muscular dystrophy-dystroglycanopathy type B5
|
0110635 |
| C0270962 |
Multi-core congenital myopathy |
DO |
muscular dystrophy-dystroglycanopathy type B6
|
0110637 |
| C0270962 |
Multi-core congenital myopathy |
DO |
congenital muscular dystrophy due to integrin alpha-7 deficiency
|
0110639 |
| C0270962 |
Multi-core congenital myopathy |
DO |
congenital muscular dystrophy due to LMNA mutation
|
0110640 |
| C0270962 |
Multi-core congenital myopathy |
DO |
nemaline myopathy
|
3191 |
| C0270962 |
Multi-core congenital myopathy |
DO |
central core myopathy
|
3529 |
| C0270962 |
Multi-core congenital myopathy |
ICD10CM |
Nemaline myopathy
|
G71.2 |
| C0270962 |
Multi-core congenital myopathy |
ICD10CM |
Congenital myopathies
|
G71.2 |
| C0270962 |
Multi-core congenital myopathy |
ICD10CM |
Multicore disease
|
G71.2 |
| C0270962 |
Multi-core congenital myopathy |
ICD10CM |
Minicore disease
|
G71.2 |
| C0270962 |
Multi-core congenital myopathy |
ICD10CM |
Fiber-type disproportion
|
G71.2 |
| C0270962 |
Multi-core congenital myopathy |
ICD10CM |
Central core disease
|
G71.2 |
| C0270962 |
Multi-core congenital myopathy |
ICD10CM |
Myotubular (centronuclear) myopathy
|
G71.2 |
| C0270962 |
Multi-core congenital myopathy |
MONDO |
megaconial type congenital muscular dystrophy
|
0011246 |
| C0270962 |
Multi-core congenital myopathy |
MONDO |
congenital muscular dystrophy 1B
|
0011486 |
| C0270962 |
Multi-core congenital myopathy |
MONDO |
muscular dystrophy-dystroglycanopathy type B5
|
0011688 |
| C0270962 |
Multi-core congenital myopathy |
MONDO |
muscular dystrophy-dystroglycanopathy type B6
|
0012138 |
| C0270962 |
Multi-core congenital myopathy |
MONDO |
congenital muscular dystrophy due to integrin alpha-7 deficiency
|
0013177 |
| C0270962 |
Multi-core congenital myopathy |
MONDO |
congenital muscular dystrophy due to LMNA mutation
|
0013178 |
| C0270962 |
Multi-core congenital myopathy |
MONDO |
muscular dystrophy-dystroglycanopathy
|
0018276 |
| C0270962 |
Multi-core congenital myopathy |
MONDO |
multiminicore myopathy
|
0018948 |