C1842160 |
MYOPATHY, MYOSIN STORAGE (disorder) |
DO |
autosomal dominant hyaline body myopathy
|
0111269 |
C1842160 |
MYOPATHY, MYOSIN STORAGE (disorder) |
MONDO |
myopathy, myosin storage, autosomal dominant
|
0012018 |
C1842160 |
MYOPATHY, MYOSIN STORAGE (disorder) |
MSH |
Myopathy, Hyaline Body, Autosomal Dominant
|
C564253 |
C1842160 |
MYOPATHY, MYOSIN STORAGE (disorder) |
MSH |
Myopathy, Myosin Storage
|
C564253 |
C1842160 |
MYOPATHY, MYOSIN STORAGE (disorder) |
OMIM |
MSMA
|
608358 |
C1842160 |
MYOPATHY, MYOSIN STORAGE (disorder) |
OMIM |
MYOPATHY, MYOSIN STORAGE, AUTOSOMAL DOMINANT
|
608358 |