| C1834339 |
Myopathy, Actin, Congenital, with Excess of Thin Myofilaments |
DO |
Van der Woude syndrome
|
0060239 |
| C1834339 |
Myopathy, Actin, Congenital, with Excess of Thin Myofilaments |
DO |
nemaline myopathy 3
|
0110927 |
| C1834339 |
Myopathy, Actin, Congenital, with Excess of Thin Myofilaments |
MONDO |
nemaline myopathy 3
|
0008070 |
| C1834339 |
Myopathy, Actin, Congenital, with Excess of Thin Myofilaments |
MONDO |
nemaline myopathy
|
0018958 |
| C1834339 |
Myopathy, Actin, Congenital, with Excess of Thin Myofilaments |
MONDO |
van der Woude syndrome
|
0019508 |
| C1834339 |
Myopathy, Actin, Congenital, with Excess of Thin Myofilaments |
MSH |
Myopathy, Actin, Congenital, with Excess of Thin Myofilaments
|
C563529 |
| C1834339 |
Myopathy, Actin, Congenital, with Excess of Thin Myofilaments |
OMIM |
MYOPATHY, ACTIN, CONGENITAL, WITH EXCESS OF THIN MYOFILAMENTS
|
161800 |
| C1834339 |
Myopathy, Actin, Congenital, with Excess of Thin Myofilaments |
OMIM |
NEMALINE MYOPATHY 3, WITH INTRANUCLEAR RODS
|
161800 |
| C1834339 |
Myopathy, Actin, Congenital, with Excess of Thin Myofilaments |
OMIM |
MYOPATHY, ACTIN, CONGENITAL, WITH CORES
|
161800 |
| C1834339 |
Myopathy, Actin, Congenital, with Excess of Thin Myofilaments |
OMIM |
NEMALINE MYOPATHY 3
|
161800 |
| C1834339 |
Myopathy, Actin, Congenital, with Excess of Thin Myofilaments |
OMIM |
NEM3
|
161800 |