|
glycogenosis due to glycogen branching enzyme deficiency
|
C0017923 |
|
|
Cirrhosis, familial, with deposition of abnormal glycogen
|
C0017923 |
|
|
cirrhosis, familial, with deposition of abnormal glycogen
|
C0017923 |
|
|
GSD IV, neuromuscular form, adult, with isolated myopathy
|
C0017923 |
|
|
GSD IV, neuromuscular form, childhood
|
C0017923 |
|
|
GSD IV, neuromuscular form, congenital
|
C0017923 |
|
|
GSD IV, neuromuscular form, fatal perinatal
|
C0017923 |
|
|
Brancher deficiency glycogen storage disease
|
C0017923 |
|
|
Branching-transferase deficiency glycogenosis
|
C0017923 |
|
|
brancher deficiency glycogenosis
|
C0017923 |
|
|
branching-transferase deficiency glycogenosis
|
C0017923 |
|
|
GSD IV, nonprogressive hepatic
|
C0017923 |
|
