| C1856304 |
GSD IV, Neuromuscular Form, Congenital |
DO |
glycogen storage disease IV
|
2750 |
| C1856304 |
GSD IV, Neuromuscular Form, Congenital |
MONDO |
glycogen storage disease due to glycogen branching enzyme deficiency
|
0009292 |
| C1856304 |
GSD IV, Neuromuscular Form, Congenital |
MONDO |
glycogen storage disease due to glycogen branching enzyme deficiency, congenital neuromuscular form
|
0017698 |
| C1856304 |
GSD IV, Neuromuscular Form, Congenital |
MSH |
GSD IV, Neuromuscular Form, Congenital
|
C565542 |
| C1856304 |
GSD IV, Neuromuscular Form, Congenital |
OMIM |
GLYCOGEN STORAGE DISEASE IV
|
232500 |
| C1856304 |
GSD IV, Neuromuscular Form, Congenital |
OMIM |
AMYLOPECTINOSIS
|
232500 |
| C1856304 |
GSD IV, Neuromuscular Form, Congenital |
OMIM |
GSD IV, CLASSIC HEPATIC
|
232500 |
| C1856304 |
GSD IV, Neuromuscular Form, Congenital |
OMIM |
GSD IV, NEUROMUSCULAR FORM, FATAL PERINATAL
|
232500 |
| C1856304 |
GSD IV, Neuromuscular Form, Congenital |
OMIM |
GSD IV, NEUROMUSCULAR FORM, CONGENITAL
|
232500 |
| C1856304 |
GSD IV, Neuromuscular Form, Congenital |
OMIM |
GSD IV, NEUROMUSCULAR FORM, CHILDHOOD
|
232500 |
| C1856304 |
GSD IV, Neuromuscular Form, Congenital |
ORDO |
Glycogen storage disease due to glycogen branching enzyme deficiency, congenital neuromuscular form
|
308670 |