Category: E74 - Other disorders of carbohydrate metabolism

 Chapter Notes

 Section Notes

 E74

Other disorders of carbohydrate metabolism

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

Code also, 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

muscle phosphofructokinase deficiency (E74.09)

 E74.10

Disorder of fructose metabolism, unspecified

 E74.11

Essential fructosuria

Fructokinase deficiency

 E74.12

Hereditary fructose intolerance

Fructosemia

 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

Galactokinase deficiency

 E74.3

Other disorders of intestinal carbohydrate absorption

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

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

Essential pentosuria

 E74.9

Disorder of carbohydrate metabolism, unspecified