E74 |
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Other disorders of carbohydrate metabolism  |
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Excludes1 |
diabetes mellitus (E08-E13) hypoglycemia NOS (E16.2) increased secretion of glucagon (E16.3) mucopolysaccharidosis (E76.0-E76.3)
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E74.0 |
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Glycogen storage disease |
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E74.00 |
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Glycogen storage disease, unspecified |
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E74.01 |
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von Gierke disease |
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Type I glycogen storage disease |
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E74.02 |
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Pompe disease |
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Cardiac glycogenosis | Type II glycogen storage disease |
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E74.03 |
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Cori disease |
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Forbes disease | Type III glycogen storage disease |
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E74.04 |
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McArdle disease |
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Type V glycogen storage disease |
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E74.05 |
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Lysosome-associated membrane protein 2 [LAMP2] deficiency |
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Danon disease |
CodeAlso |
, if applicable, associated manifestations such as: dilated cardiomyopathy (I42.0) obstructive hypertrophic cardiomyopathy (I42.1)
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E74.09 |
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Other glycogen storage disease |
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Andersen disease | Glycogen storage disease, types 0, IV, VI-XI | Hers disease | Liver phosphorylase deficiency | Muscle phosphofructokinase deficiency | Tauri disease |
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E74.1 |
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Disorders of fructose metabolism |
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Excludes1 |
muscle phosphofructokinase deficiency (E74.09)
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E74.10 |
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Disorder of fructose metabolism, unspecified |
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E74.11 |
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Essential fructosuria |
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E74.12 |
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Hereditary fructose intolerance |
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E74.19 |
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Other disorders of fructose metabolism |
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Fructose-1, 6-diphosphatase deficiency |
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E74.2 |
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Disorders of galactose metabolism |
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E74.20 |
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Disorders of galactose metabolism, unspecified |
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E74.21 |
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Galactosemia |
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E74.29 |
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Other disorders of galactose metabolism |
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E74.3 |
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Other disorders of intestinal carbohydrate absorption |
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Excludes2 |
lactose intolerance (E73.-)
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E74.31 |
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Sucrase-isomaltase deficiency |
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E74.39 |
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Other disorders of intestinal carbohydrate absorption |
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Disorder of intestinal carbohydrate absorption NOS | Glucose-galactose malabsorption | Sucrase deficiency |
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E74.4 |
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Disorders of pyruvate metabolism and gluconeogenesis |
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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)
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E74.8 |
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Other specified disorders of carbohydrate metabolism |
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E74.81 |
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Disorders of glucose transport, not elsewhere classified |
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E74.810 |
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Glucose transporter protein type 1 deficiency |
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De Vivo syndrome | Glucose transport defect, blood-brain barrier | Glut1 deficiency | GLUT1 deficiency syndrome 1, infantile onset | GLUT1 deficiency syndrome 2, childhood onset |
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E74.818 |
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Other disorders of glucose transport |
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(Familial) renal glycosuria |
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E74.819 |
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Disorders of glucose transport, unspecified |
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E74.82 |
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Disorders of citrate metabolism |
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E74.820 |
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SLC13A5 Citrate Transporter Disorder |
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E74.829 |
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Other disorders of citrate metabolism |
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E74.89 |
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Other specified disorders of carbohydrate metabolism |
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E74.9 |
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Disorder of carbohydrate metabolism, unspecified |
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