<https://averbis.com/icd_10_cm_2017/e74-09-branching-enzyme-deficiency/#webpage>
<http://schema.org/description>
"1,4,alpha-glucan 6-alpha-glucosyltransferase deficiency|Amylopectinosis|Andersen disease|Andersen's disease|Brancher deficiency glycogen storage disease|Branching enzyme deficiency|Branching-transferase deficiency glycogenosis|Cardiac glycogen phosphorylase kinase deficiency|Cardiac glycogen phosphorylase kinase deficiency (disorder)|Danon disease|Danon disease (disorder)|Deficiency of alpha-dextrin endo-1,6-alpha-glucosidase|Deficiency of alpha-dextrin endo-1,6-alpha-glucosidase (disorder)|Deficiency of alpha-galactosidase|Deficiency of alpha-galactosidase (disorder)|Deficiency of melibiase|Fanconi-Bickel syndrome|GSD IV|GSD VI|GSD VII|GSD VIII|GSD X|Glycogen phosphorylase kinase deficiency|Glycogen phosphorylase kinase deficiency (disorder)|Glycogen phosphorylase kinase deficiency, X-linked|Glycogen phosphorylase kinase deficiency, X-linked (disorder)|Glycogen phosphorylase kinase deficiency, autosomal recessive|Glycogen phosphorylase kinase deficiency, autosomal recessive (disorder)|Glycogen storage disease VIII|Glycogen storage disease type 0|Glycogen storage disease type 8|Glycogen storage disease type 9|Glycogen storage disease type IV|Glycogen storage disease type IX|Glycogen storage disease type Ic|Glycogen storage disease type VIII|Glycogen storage disease type VIII (disorder)|Glycogen storage disease type X|Glycogen storage disease type X (disorder)|Glycogen storage disease, hepatic form|Glycogen storage disease, hepatic form (disorder)|Glycogen storage disease, muscular form|Glycogen storage disease, muscular form (disorder)|Glycogen storage disease, type 4|Glycogen storage disease, type 7|Glycogen storage disease, type IV|Glycogen storage disease, type IV (disorder)|Glycogen storage disease, type IX|Glycogen storage disease, type IX (disorder)|Glycogen storage disease, type VI|Glycogen storage disease, type VI (disorder)|Glycogen storage disease, type VII|Glycogen storage disease, type VII (disorder)|Glycogen storage disease, types 0, IV, VI-XI|Glycogen synthase deficiency|Glycogen synthase deficiency (disorder)|Glycogenosis due to inactive hepatic glycogen phosphorylase|Glycogenosis due to inactive phosphorylase|Glycogenosis due to inactive phosphorylase AND kinase|Glycogenosis viiia|Glycogenosis with glucoaminophosphaturia|Glycogenosis with glucoaminophosphaturia (disorder)|Glycogenosis, type 4|Hepatic and muscle glycogen phosphorylase kinase deficiency|Hepatic and muscle glycogen phosphorylase kinase deficiency (disorder)|Hepatic glycogen phosphorylase deficiency|Hepatic glycogen phosphorylase kinase deficiency|Hepatic glycogen phosphorylase kinase deficiency (disorder)|Hepatic glycogenosis with de Toni-Debre-Fanconi syndrome|Hepatic glycogenosis with de Toni-DebrÃ©-Fanconi syndrome|Hepatic phosphorylase deficiency|Hepatic phosphorylase kinase deficiency|Hers disease|Liver phosphorylase deficiency|Muscle phosphofructokinase deficiency|PHK - Hepatic phosphorylase kinase deficiency|Phosphate transport defect|Phosphate transport defect (disorder)|Phosphorylase kinase deficiency of liver|Pseudo-phlorizin diabetes|Renal glucose-losing syndrome|Tarui's disease|Tauri disease"
<https://averbis.com/icd_10_cm_2017/e74-09-branching-enzyme-deficiency/>