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