C0017923 |
Glycogen Storage Disease Type IV |
DO |
glycogen storage disease VII
|
11721 |
C0017923 |
Glycogen Storage Disease Type IV |
DO |
glycogen storage disease IV
|
2750 |
C0017923 |
Glycogen Storage Disease Type IV |
DO |
glycogen storage disease VI
|
2754 |
C0017923 |
Glycogen Storage Disease Type IV |
ICD10CM |
Andersen disease
|
E74.09 |
C0017923 |
Glycogen Storage Disease Type IV |
ICD10CM |
Hers disease
|
E74.09 |
C0017923 |
Glycogen Storage Disease Type IV |
ICD10CM |
Liver phosphorylase deficiency
|
E74.09 |
C0017923 |
Glycogen Storage Disease Type IV |
ICD10CM |
Tauri disease
|
E74.09 |
C0017923 |
Glycogen Storage Disease Type IV |
ICD10CM |
Muscle phosphofructokinase deficiency
|
E74.09 |
C0017923 |
Glycogen Storage Disease Type IV |
MONDO |
glycogen storage disease due to glycogen branching enzyme deficiency
|
0009292 |
C0017923 |
Glycogen Storage Disease Type IV |
MSH |
Glycogen Storage Disease Type IV
|
D006011 |
C0017923 |
Glycogen Storage Disease Type IV |
NCI |
Glycogen Storage Disease Type IV
|
C84737 |
C0017923 |
Glycogen Storage Disease Type IV |
OMIM |
GLYCOGEN STORAGE DISEASE IV
|
232500 |
C0017923 |
Glycogen Storage Disease Type IV |
OMIM |
AMYLOPECTINOSIS
|
232500 |
C0017923 |
Glycogen Storage Disease Type IV |
OMIM |
GSD IV, CLASSIC HEPATIC
|
232500 |
C0017923 |
Glycogen Storage Disease Type IV |
OMIM |
GSD IV, NEUROMUSCULAR FORM, FATAL PERINATAL
|
232500 |
C0017923 |
Glycogen Storage Disease Type IV |
OMIM |
GSD IV, NEUROMUSCULAR FORM, CONGENITAL
|
232500 |
C0017923 |
Glycogen Storage Disease Type IV |
OMIM |
GSD IV, NEUROMUSCULAR FORM, CHILDHOOD
|
232500 |
C0017923 |
Glycogen Storage Disease Type IV |
ORDO |
Glycogen storage disease due to glycogen branching enzyme deficiency
|
367 |