| 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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