C0017925 |
Glycogen Storage Disease Type VI |
DO |
glycogen storage disease VII
|
11721 |
C0017925 |
Glycogen Storage Disease Type VI |
DO |
glycogen storage disease IV
|
2750 |
C0017925 |
Glycogen Storage Disease Type VI |
DO |
glycogen storage disease VI
|
2754 |
C0017925 |
Glycogen Storage Disease Type VI |
ICD10CM |
Andersen disease
|
E74.09 |
C0017925 |
Glycogen Storage Disease Type VI |
ICD10CM |
Hers disease
|
E74.09 |
C0017925 |
Glycogen Storage Disease Type VI |
ICD10CM |
Liver phosphorylase deficiency
|
E74.09 |
C0017925 |
Glycogen Storage Disease Type VI |
ICD10CM |
Tauri disease
|
E74.09 |
C0017925 |
Glycogen Storage Disease Type VI |
ICD10CM |
Muscle phosphofructokinase deficiency
|
E74.09 |
C0017925 |
Glycogen Storage Disease Type VI |
MONDO |
glycogen storage disease VI
|
0009294 |
C0017925 |
Glycogen Storage Disease Type VI |
MSH |
Glycogen Storage Disease Type VI
|
D006013 |
C0017925 |
Glycogen Storage Disease Type VI |
NCI |
Glycogen Storage Disease Type VI
|
C126875 |
C0017925 |
Glycogen Storage Disease Type VI |
OMIM |
GLYCOGEN STORAGE DISEASE VI
|
232700 |
C0017925 |
Glycogen Storage Disease Type VI |
OMIM |
HERS DISEASE
|
232700 |
C0017925 |
Glycogen Storage Disease Type VI |
ORDO |
Glycogen storage disease due to liver glycogen phosphorylase deficiency
|
369 |