 E74 |
 |
Other disorders of carbohydrate metabolism  |
| |
| Excludes1 |
diabetes mellitus (E08-E13)
hypoglycemia NOS (E16.2)
increased secretion of glucagon (E16.3)
mucopolysaccharidosis (E76.0-E76.3)
|
|
| |
| E74.0 |
|
Glycogen storage disease |
| |
 E74.00 |
|
Glycogen storage disease, unspecified |
| | |
| E74.01 |
|
von Gierke disease |
| |
| Type I glycogen storage disease |
|
| | |
| E74.02 |
|
Pompe disease |
| |
| Cardiac glycogenosis | | Type II glycogen storage disease |
|
| | |
| E74.03 |
|
Cori disease |
| |
| Forbes disease | | Type III glycogen storage disease |
|
| | |
| E74.04 |
|
McArdle disease |
| |
| Type V glycogen storage disease |
|
| | |
| E74.05 |
|
Lysosome-associated membrane protein 2 [LAMP2] deficiency |
| |
| Danon disease |
| CodeAlso |
, if applicable, associated manifestations such as:
dilated cardiomyopathy (I42.0)
obstructive hypertrophic cardiomyopathy (I42.1)
|
|
| | |
| E74.09 |
|
Other glycogen storage disease |
| |
| Andersen disease | | Glycogen storage disease, types 0, IV, VI-XI | | Hers disease | | Liver phosphorylase deficiency | | Muscle phosphofructokinase deficiency | | Tauri disease |
|
| |
| |
| E74.1 |
|
Disorders of fructose metabolism |
| |
| Excludes1 |
muscle phosphofructokinase deficiency (E74.09)
|
|
| |
| E74.10 |
|
Disorder of fructose metabolism, unspecified |
| | |
| E74.11 |
|
Essential fructosuria |
| |
|
| | |
| E74.12 |
|
Hereditary fructose intolerance |
| |
|
| | |
| E74.19 |
|
Other disorders of fructose metabolism |
| |
| Fructose-1, 6-diphosphatase deficiency |
|
| |
| |
| E74.2 |
|
Disorders of galactose metabolism |
| |
| E74.20 |
|
Disorders of galactose metabolism, unspecified |
| | |
| E74.21 |
|
Galactosemia |
| | |
| E74.29 |
|
Other disorders of galactose metabolism |
| |
|
| |
| |
| E74.3 |
|
Other disorders of intestinal carbohydrate absorption |
| |
| Excludes2 |
lactose intolerance (E73.-)
|
|
| |
| E74.31 |
|
Sucrase-isomaltase deficiency |
| | |
| E74.39 |
|
Other disorders of intestinal carbohydrate absorption |
| |
| Disorder of intestinal carbohydrate absorption NOS | | Glucose-galactose malabsorption | | Sucrase deficiency |
|
| |
| |
| E74.4 |
|
Disorders of pyruvate metabolism and gluconeogenesis |
| |
| Deficiency of phosphoenolpyruvate carboxykinase | | Deficiency of pyruvate carboxylase | | Deficiency of pyruvate dehydrogenase |
| Excludes1 |
disorders of pyruvate metabolism and gluconeogenesis with anemia (D55.-)
Leigh's syndrome (G31.82)
|
|
|
| |
| E74.8 |
|
Other specified disorders of carbohydrate metabolism |
| |
| E74.81 |
|
Disorders of glucose transport, not elsewhere classified |
| |
| E74.810 |
|
Glucose transporter protein type 1 deficiency |
| |
| De Vivo syndrome | | Glucose transport defect, blood-brain barrier | | Glut1 deficiency | | GLUT1 deficiency syndrome 1, infantile onset | | GLUT1 deficiency syndrome 2, childhood onset |
|
| | |
| E74.818 |
|
Other disorders of glucose transport |
| |
| (Familial) renal glycosuria |
|
| | |
| E74.819 |
|
Disorders of glucose transport, unspecified |
| | | |
| E74.89 |
|
Other specified disorders of carbohydrate metabolism |
| |
|
| |
| |
| E74.9 |
|
Disorder of carbohydrate metabolism, unspecified |
|