ICD-10-CM › E
ICD-10-CM codes starting with E
1,270 codes, page 11 of 13. Every code ever valid for billing is listed, including those now retired.
| Code | Description | Status |
|---|---|---|
| E72.8 | Other specified disorders of amino-acid metabolism | Not billable |
| E72.81 | Disorders of gamma aminobutyric acid metabolism | Valid |
| E72.89 | Other specified disorders of amino-acid metabolism | Valid |
| E72.9 | Disorder of amino-acid metabolism, unspecified | Valid |
| E73 | Lactose intolerance | Not billable |
| E73.0 | Congenital lactase deficiency | Valid |
| E73.1 | Secondary lactase deficiency | Valid |
| E73.8 | Other lactose intolerance | Valid |
| E73.9 | Lactose intolerance, unspecified | Valid |
| E74 | Other disorders of carbohydrate metabolism | Not billable |
| E74.0 | Glycogen storage disease | Not billable |
| E74.00 | Glycogen storage disease, unspecified | Valid |
| E74.01 | von Gierke disease | Valid |
| E74.02 | Pompe disease | Valid |
| E74.03 | Cori disease | Valid |
| E74.04 | McArdle disease | Valid |
| E74.05 | Lysosome-associated membrane protein 2 [LAMP2] deficiency | Valid |
| E74.09 | Other glycogen storage disease | Valid |
| E74.1 | Disorders of fructose metabolism | Not billable |
| E74.10 | Disorder of fructose metabolism, unspecified | Valid |
| E74.11 | Essential fructosuria | Valid |
| E74.12 | Hereditary fructose intolerance | Valid |
| E74.19 | Other disorders of fructose metabolism | Valid |
| E74.2 | Disorders of galactose metabolism | Not billable |
| E74.20 | Disorders of galactose metabolism, unspecified | Valid |
| E74.21 | Galactosemia | Valid |
| E74.29 | Other disorders of galactose metabolism | Valid |
| E74.3 | Other disorders of intestinal carbohydrate absorption | Not billable |
| E74.31 | Sucrase-isomaltase deficiency | Valid |
| E74.39 | Other disorders of intestinal carbohydrate absorption | Valid |
| E74.4 | Disorders of pyruvate metabolism and gluconeogenesis | Valid |
| E74.8 | Other specified disorders of carbohydrate metabolism | Not billable |
| E74.81 | Disorders of glucose transport, not elsewhere classified | Not billable |
| E74.810 | Glucose transporter protein type 1 deficiency | Valid |
| E74.818 | Other disorders of glucose transport | Valid |
| E74.819 | Disorders of glucose transport, unspecified | Valid |
| E74.82 | Disorders of citrate metabolism | Not billable |
| E74.820 | SLC13A5 Citrate Transporter Disorder | Valid |
| E74.829 | Other disorders of citrate metabolism | Valid |
| E74.89 | Other specified disorders of carbohydrate metabolism | Valid |
| E74.9 | Disorder of carbohydrate metabolism, unspecified | Valid |
| E75 | Disorders of sphingolipid metabolism and other lipid storage disorders | Not billable |
| E75.0 | GM2 gangliosidosis | Not billable |
| E75.00 | GM2 gangliosidosis, unspecified | Valid |
| E75.01 | Sandhoff disease | Valid |
| E75.02 | Tay-Sachs disease | Valid |
| E75.09 | Other GM2 gangliosidosis | Valid |
| E75.1 | Other and unspecified gangliosidosis | Not billable |
| E75.10 | Unspecified gangliosidosis | Valid |
| E75.11 | Mucolipidosis IV | Valid |
| E75.19 | Other gangliosidosis | Valid |
| E75.2 | Other sphingolipidosis | Not billable |
| E75.21 | Fabry (-Anderson) disease | Valid |
| E75.22 | Gaucher disease | Valid |
| E75.23 | Krabbe disease | Valid |
| E75.24 | Niemann-Pick disease | Not billable |
| E75.240 | Niemann-Pick disease type A | Valid |
| E75.241 | Niemann-Pick disease type B | Valid |
| E75.242 | Niemann-Pick disease type C | Valid |
| E75.243 | Niemann-Pick disease type D | Valid |
| E75.244 | Niemann-Pick disease type A/B | Valid |
| E75.248 | Other Niemann-Pick disease | Valid |
| E75.249 | Niemann-Pick disease, unspecified | Valid |
| E75.25 | Metachromatic leukodystrophy | Valid |
| E75.26 | Sulfatase deficiency | Valid |
| E75.27 | Pelizaeus-Merzbacher disease | Valid |
| E75.28 | Canavan disease | Valid |
| E75.29 | Other sphingolipidosis | Valid |
| E75.3 | Sphingolipidosis, unspecified | Valid |
| E75.4 | Neuronal ceroid lipofuscinosis | Valid |
| E75.5 | Other lipid storage disorders | Valid |
| E75.6 | Lipid storage disorder, unspecified | Valid |
| E76 | Disorders of glycosaminoglycan metabolism | Not billable |
| E76.0 | Mucopolysaccharidosis, type I | Not billable |
| E76.01 | Hurler's syndrome | Valid |
| E76.02 | Hurler-Scheie syndrome | Valid |
| E76.03 | Scheie's syndrome | Valid |
| E76.1 | Mucopolysaccharidosis, type II | Valid |
| E76.2 | Other mucopolysaccharidoses | Not billable |
| E76.21 | Morquio mucopolysaccharidoses | Not billable |
| E76.210 | Morquio A mucopolysaccharidoses | Valid |
| E76.211 | Morquio B mucopolysaccharidoses | Valid |
| E76.219 | Morquio mucopolysaccharidoses, unspecified | Valid |
| E76.22 | Sanfilippo mucopolysaccharidoses | Valid |
| E76.29 | Other mucopolysaccharidoses | Valid |
| E76.3 | Mucopolysaccharidosis, unspecified | Valid |
| E76.8 | Other disorders of glucosaminoglycan metabolism | Valid |
| E76.9 | Glucosaminoglycan metabolism disorder, unspecified | Valid |
| E77 | Disorders of glycoprotein metabolism | Not billable |
| E77.0 | Defects in post-translational modification of lysosomal enzymes | Valid |
| E77.1 | Defects in glycoprotein degradation | Valid |
| E77.8 | Other disorders of glycoprotein metabolism | Valid |
| E77.9 | Disorder of glycoprotein metabolism, unspecified | Valid |
| E78 | Disorders of lipoprotein metabolism and other lipidemias | Not billable |
| E78.0 | Pure hypercholesterolemia | Not billable |
| E78.00 | Pure hypercholesterolemia, unspecified | Valid |
| E78.01 | Familial hypercholesterolemia | Not billable |
| E78.010 | Homozygous familial hypercholesterolemia [HoFH] | Valid |
| E78.011 | Heterozygous familial hypercholesterolemia [HeFH] | Valid |
| E78.019 | Familial hypercholesterolemia, unspecified | Valid |