ICD-10-CM › E
ICD-10-CM codes starting with E
1,270 codes, page 12 of 13. Every code ever valid for billing is listed, including those now retired.
| Code | Description | Status |
|---|---|---|
| E78.1 | Pure hyperglyceridemia | Valid |
| E78.2 | Mixed hyperlipidemia | Valid |
| E78.3 | Hyperchylomicronemia | Valid |
| E78.4 | Other hyperlipidemia | Not billable |
| E78.41 | Elevated Lipoprotein(a) | Valid |
| E78.49 | Other hyperlipidemia | Valid |
| E78.5 | Hyperlipidemia, unspecified | Valid |
| E78.6 | Lipoprotein deficiency | Valid |
| E78.7 | Disorders of bile acid and cholesterol metabolism | Not billable |
| E78.70 | Disorder of bile acid and cholesterol metabolism, unspecified | Valid |
| E78.71 | Barth syndrome | Valid |
| E78.72 | Smith-Lemli-Opitz syndrome | Valid |
| E78.79 | Other disorders of bile acid and cholesterol metabolism | Valid |
| E78.8 | Other disorders of lipoprotein metabolism | Not billable |
| E78.81 | Lipoid dermatoarthritis | Valid |
| E78.89 | Other lipoprotein metabolism disorders | Valid |
| E78.9 | Disorder of lipoprotein metabolism, unspecified | Valid |
| E79 | Disorders of purine and pyrimidine metabolism | Not billable |
| E79.0 | Hyperuricemia without signs of inflammatory arthritis and tophaceous disease | Valid |
| E79.1 | Lesch-Nyhan syndrome | Valid |
| E79.2 | Myoadenylate deaminase deficiency | Valid |
| E79.8 | Other disorders of purine and pyrimidine metabolism | Not billable |
| E79.81 | Aicardi-Goutieres syndrome | Valid |
| E79.82 | Hereditary xanthinuria | Valid |
| E79.89 | Other specified disorders of purine and pyrimidine metabolism | Valid |
| E79.9 | Disorder of purine and pyrimidine metabolism, unspecified | Valid |
| E80 | Disorders of porphyrin and bilirubin metabolism | Not billable |
| E80.0 | Hereditary erythropoietic porphyria | Valid |
| E80.1 | Porphyria cutanea tarda | Valid |
| E80.2 | Other and unspecified porphyria | Not billable |
| E80.20 | Unspecified porphyria | Valid |
| E80.21 | Acute intermittent (hepatic) porphyria | Valid |
| E80.29 | Other porphyria | Valid |
| E80.3 | Defects of catalase and peroxidase | Valid |
| E80.4 | Gilbert syndrome | Valid |
| E80.5 | Crigler-Najjar syndrome | Valid |
| E80.6 | Other disorders of bilirubin metabolism | Valid |
| E80.7 | Disorder of bilirubin metabolism, unspecified | Valid |
| E83 | Disorders of mineral metabolism | Not billable |
| E83.0 | Disorders of copper metabolism | Not billable |
| E83.00 | Disorder of copper metabolism, unspecified | Valid |
| E83.01 | Wilson's disease | Valid |
| E83.09 | Other disorders of copper metabolism | Valid |
| E83.1 | Disorders of iron metabolism | Not billable |
| E83.10 | Disorder of iron metabolism, unspecified | Valid |
| E83.11 | Hemochromatosis | Not billable |
| E83.110 | Hereditary hemochromatosis | Valid |
| E83.111 | Hemochromatosis due to repeated red blood cell transfusions | Valid |
| E83.118 | Other hemochromatosis | Valid |
| E83.119 | Hemochromatosis, unspecified | Valid |
| E83.19 | Other disorders of iron metabolism | Valid |
| E83.2 | Disorders of zinc metabolism | Valid |
| E83.3 | Disorders of phosphorus metabolism and phosphatases | Not billable |
| E83.30 | Disorder of phosphorus metabolism, unspecified | Valid |
| E83.31 | Familial hypophosphatemia | Valid |
| E83.32 | Hereditary vitamin D-dependent rickets (type 1) (type 2) | Valid |
| E83.39 | Other disorders of phosphorus metabolism | Valid |
| E83.4 | Disorders of magnesium metabolism | Not billable |
| E83.40 | Disorders of magnesium metabolism, unspecified | Valid |
| E83.41 | Hypermagnesemia | Valid |
| E83.42 | Hypomagnesemia | Valid |
| E83.49 | Other disorders of magnesium metabolism | Valid |
| E83.5 | Disorders of calcium metabolism | Not billable |
| E83.50 | Unspecified disorder of calcium metabolism | Valid |
| E83.51 | Hypocalcemia | Valid |
| E83.52 | Hypercalcemia | Valid |
| E83.59 | Other disorders of calcium metabolism | Valid |
| E83.8 | Other disorders of mineral metabolism | Not billable |
| E83.81 | Hungry bone syndrome | Valid |
| E83.82 | Disorders of pyrophosphate metabolism | Not billable |
| E83.820 | Generalized arterial calcification of infancy with unspecified genetic causality | Valid |
| E83.821 | ENPP1 deficiency causing generalized arterial calcification of infancy | Valid |
| E83.822 | ENPP1 deficiency causing autosomal recessive hypophosphatemic rickets type 2 | Valid |
| E83.823 | ABCC6 deficiency causing generalized arterial calcification of infancy | Valid |
| E83.824 | ABCC6 deficiency causing pseudoxanthoma elasticum | Valid |
| E83.825 | CD73 deficiency causing arterial calcification | Valid |
| E83.89 | Other disorders of mineral metabolism | Valid |
| E83.9 | Disorder of mineral metabolism, unspecified | Valid |
| E84 | Cystic fibrosis | Not billable |
| E84.0 | Cystic fibrosis with pulmonary manifestations | Valid |
| E84.1 | Cystic fibrosis with intestinal manifestations | Not billable |
| E84.11 | Meconium ileus in cystic fibrosis | Valid |
| E84.19 | Cystic fibrosis with other intestinal manifestations | Valid |
| E84.8 | Cystic fibrosis with other manifestations | Valid |
| E84.9 | Cystic fibrosis, unspecified | Valid |
| E85 | Amyloidosis | Not billable |
| E85.0 | Non-neuropathic heredofamilial amyloidosis | Valid |
| E85.1 | Neuropathic heredofamilial amyloidosis | Valid |
| E85.2 | Heredofamilial amyloidosis, unspecified | Valid |
| E85.3 | Secondary systemic amyloidosis | Valid |
| E85.4 | Organ-limited amyloidosis | Valid |
| E85.8 | Other amyloidosis | Not billable |
| E85.81 | Light chain (AL) amyloidosis | Valid |
| E85.82 | Wild-type transthyretin-related (ATTR) amyloidosis | Valid |
| E85.89 | Other amyloidosis | Valid |
| E85.9 | Amyloidosis, unspecified | Valid |
| E86 | Volume depletion | Not billable |
| E86.0 | Dehydration | Valid |
| E86.1 | Hypovolemia | Valid |
| E86.9 | Volume depletion, unspecified | Valid |