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ICD-10-CM-2023 Diagnosis Codes Overview
ICD-10-CM-2023 > E00-E89 > E70-E88 > E74
E70-E88
Metabolic disorders
Excl1.:
androgen insensitivity syndrome (E34.5-)
congenital adrenal hyperplasia (E25.0)
hemolytic anemias attributable to enzyme disorders (D55.-)
Marfan's syndrome (Q87.4)
5-alpha-reductase deficiency (E29.1)
Excl2.:
Ehlers-Danlos syndromes (Q79.6-)
E74

Other disorders of carbohydrate metabolism

Excl1.:
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
Info:
Type I glycogen storage disease
E74.02
Pompe disease
Info:
Cardiac glycogenosis
Type II glycogen storage disease
E74.03
Cori disease
Info:
Forbes disease
Type III glycogen storage disease
E74.04
McArdle disease
Info:
Type V glycogen storage disease
E74.09
Other glycogen storage disease
Info:
Andersen disease
Hers disease
Tauri disease
Glycogen storage disease, types 0, IV, VI-XI
Liver phosphorylase deficiency
Muscle phosphofructokinase deficiency
E74.1

Disorders of fructose metabolism

Excl1.:
muscle phosphofructokinase deficiency (E74.09)
E74.10
Disorder of fructose metabolism, unspecified
E74.11
Essential fructosuria
Info:
Fructokinase deficiency
E74.12
Hereditary fructose intolerance
Info:
Fructosemia
E74.19
Other disorders of fructose metabolism
Info:
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
Info:
Galactokinase deficiency
E74.3

Other disorders of intestinal carbohydrate absorption

Excl2.:
lactose intolerance (E73.-)
E74.31
Sucrase-isomaltase deficiency
E74.39
Other disorders of intestinal carbohydrate absorption
Info:
Disorder of intestinal carbohydrate absorption NOS
Glucose-galactose malabsorption
Sucrase deficiency
E74.4
Disorders of pyruvate metabolism and gluconeogenesis
Info:
Deficiency of phosphoenolpyruvate carboxykinase
Deficiency of pyruvate carboxylase
Deficiency of pyruvate dehydrogenase
Excl1.:
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
Info:
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
Info:
(Familial) renal glycosuria
E74.819
Disorders of glucose transport, unspecified
E74.89
Other specified disorders of carbohydrate metabolism
Info:
Essential pentosuria
E74.9
Disorder of carbohydrate metabolism, unspecified

 

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