C0017921 |
Glycogen storage disease type II |
DO |
glycogen storage disease II
|
2752 |
C0017921 |
Glycogen storage disease type II |
ICD10CM |
Pompe disease
|
E74.02 |
C0017921 |
Glycogen storage disease type II |
ICD10CM |
Cardiac glycogenosis
|
E74.02 |
C0017921 |
Glycogen storage disease type II |
ICD10CM |
Type II glycogen storage disease
|
E74.02 |
C0017921 |
Glycogen storage disease type II |
MONDO |
glycogen storage disease II
|
0009290 |
C0017921 |
Glycogen storage disease type II |
MSH |
Glycogen Storage Disease Type II
|
D006009 |
C0017921 |
Glycogen storage disease type II |
MSH |
Alpha-1,4-Glucosidase Deficiency
|
D006009 |
C0017921 |
Glycogen storage disease type II |
MSH |
Adult Glycogen Storage Disease Type II
|
D006009 |
C0017921 |
Glycogen storage disease type II |
MSH |
Glycogen Storage Disease Type II, Infantile
|
D006009 |
C0017921 |
Glycogen storage disease type II |
MSH |
Glycogen Storage Disease Type II, Juvenile
|
D006009 |
C0017921 |
Glycogen storage disease type II |
NCI |
Glycogen Storage Disease Type II
|
C84734 |
C0017921 |
Glycogen storage disease type II |
OMIM |
GLYCOGEN STORAGE DISEASE II
|
232300 |
C0017921 |
Glycogen storage disease type II |
OMIM |
POMPE DISEASE
|
232300 |
C0017921 |
Glycogen storage disease type II |
ORDO |
Glycogen storage disease due to acid maltase deficiency
|
365 |