2025 ICD-10 CM DIAGNOSIS INDEX TERMS STARTING WITH E
- Branched-chain organic acidurias - E71.11
- Isovaleric acidemia - E71.110
- 3-methylglutaconic aciduria - E71.111
- Other branched-chain organic acidurias - E71.118
- Disorders of propionate metabolism - E71.12
- Methylmalonic acidemia - E71.120
- Propionic acidemia - E71.121
- Other disorders of propionate metabolism - E71.128
- Other disorders of branched-chain amino-acid metabolism - E71.19
- Disorder of branched-chain amino-acid metabolism, unspecified - E71.2
- Disorders of fatty-acid metabolism - E71.3
- Disorder of fatty-acid metabolism, unspecified - E71.30
- Disorders of fatty-acid oxidation - E71.31
- Long chain/very long chain acyl CoA dehydrogenase deficiency - E71.310
- Medium chain acyl CoA dehydrogenase deficiency - E71.311
- Short chain acyl CoA dehydrogenase deficiency - E71.312
- Glutaric aciduria type II - E71.313
- Muscle carnitine palmitoyltransferase deficiency - E71.314
- Other disorders of fatty-acid oxidation - E71.318
- Disorders of ketone metabolism - E71.32
- Other disorders of fatty-acid metabolism - E71.39
- Disorders of carnitine metabolism - E71.4
- Disorder of carnitine metabolism, unspecified - E71.40
- Primary carnitine deficiency - E71.41
- Carnitine deficiency due to inborn errors of metabolism - E71.42
- Iatrogenic carnitine deficiency - E71.43
- Other secondary carnitine deficiency - E71.44
- Ruvalcaba-Myhre-Smith syndrome - E71.440
- Other secondary carnitine deficiency - E71.448
- Peroxisomal disorders - E71.5
- Peroxisomal disorder, unspecified - E71.50
- Disorders of peroxisome biogenesis - E71.51
- Zellweger syndrome - E71.510
- Neonatal adrenoleukodystrophy - E71.511
- Other disorders of peroxisome biogenesis - E71.518
- X-linked adrenoleukodystrophy - E71.52
- Childhood cerebral X-linked adrenoleukodystrophy - E71.520
- Adolescent X-linked adrenoleukodystrophy - E71.521
- Adrenomyeloneuropathy - E71.522
- Other X-linked adrenoleukodystrophy - E71.528
- X-linked adrenoleukodystrophy, unspecified type - E71.529
- Other group 2 peroxisomal disorders - E71.53
- Other peroxisomal disorders - E71.54
- Rhizomelic chondrodysplasia punctata - E71.540
- Zellweger-like syndrome - E71.541
- Other group 3 peroxisomal disorders - E71.542
- Other peroxisomal disorders - E71.548
- Disorders of amino-acid transport - E72.0
- Disorders of amino-acid transport, unspecified - E72.00
- Cystinuria - E72.01
- Hartnup's disease - E72.02
- Lowe's syndrome - E72.03
- Cystinosis - E72.04
- Other disorders of amino-acid transport - E72.09
- Disorders of sulfur-bearing amino-acid metabolism - E72.1
- Disorders of sulfur-bearing amino-acid metabolism, unspecified - E72.10
- Homocystinuria - E72.11
- Methylenetetrahydrofolate reductase deficiency - E72.12
- Other disorders of sulfur-bearing amino-acid metabolism - E72.19
- Disorders of urea cycle metabolism - E72.2
- Disorder of urea cycle metabolism, unspecified - E72.20
- Argininemia - E72.21
- Arginosuccinic aciduria - E72.22
- Citrullinemia - E72.23
- Other disorders of urea cycle metabolism - E72.29
- Disorders of lysine and hydroxylysine metabolism - E72.3
- Disorders of ornithine metabolism - E72.4
- Disorders of glycine metabolism - E72.5
- Disorder of glycine metabolism, unspecified - E72.50
- Non-ketotic hyperglycinemia - E72.51
- Trimethylaminuria - E72.52
- Primary hyperoxaluria - E72.53
- Other disorders of glycine metabolism - E72.59
- Other specified disorders of amino-acid metabolism - E72.8
- Disorders of gamma aminobutyric acid metabolism - E72.81
- Other specified disorders of amino-acid metabolism - E72.89
- Disorder of amino-acid metabolism, unspecified - E72.9
- Congenital lactase deficiency - E73.0
- Secondary lactase deficiency - E73.1
- Other lactose intolerance - E73.8
- Lactose intolerance, unspecified - E73.9
- Glycogen storage disease - E74.0
- Glycogen storage disease, unspecified - E74.00
- von Gierke disease - E74.01
- Pompe disease - E74.02
- Cori disease - E74.03
- McArdle disease - E74.04
- Lysosome-associated membrane protein 2 [LAMP2] deficiency - E74.05
- Other glycogen storage disease - E74.09
- Disorders of fructose metabolism - E74.1
- Disorder of fructose metabolism, unspecified - E74.10
- Essential fructosuria - E74.11
- Hereditary fructose intolerance - E74.12
- Other disorders of fructose metabolism - E74.19
- Disorders of galactose metabolism - E74.2
- Disorders of galactose metabolism, unspecified - E74.20
- Galactosemia - E74.21
- Other disorders of galactose metabolism - E74.29
- Other disorders of intestinal carbohydrate absorption - E74.3
- Sucrase-isomaltase deficiency - E74.31