| C2674259 |
NEUROMUSCULAR DISEASE, CONGENITAL, WITH UNIFORM TYPE 1 FIBER (disorder) |
DO |
central core myopathy
|
3529 |
| C2674259 |
NEUROMUSCULAR DISEASE, CONGENITAL, WITH UNIFORM TYPE 1 FIBER (disorder) |
MONDO |
central core myopathy
|
0007294 |
| C2674259 |
NEUROMUSCULAR DISEASE, CONGENITAL, WITH UNIFORM TYPE 1 FIBER (disorder) |
MSH |
CNMDU1
|
C567162 |
| C2674259 |
NEUROMUSCULAR DISEASE, CONGENITAL, WITH UNIFORM TYPE 1 FIBER (disorder) |
MSH |
Neuromuscular Disease, Congenital, With Uniform Type 1 Fiber
|
C567162 |
| C2674259 |
NEUROMUSCULAR DISEASE, CONGENITAL, WITH UNIFORM TYPE 1 FIBER (disorder) |
ORDO |
Central core disease
|
597 |