2025 ICD-10 CM DIAGNOSIS INDEX TERMS STARTING WITH E

  • Other disorders of intestinal carbohydrate absorption - E74.39
  • Disorders of pyruvate metabolism and gluconeogenesis - E74.4
  • Other specified disorders of carbohydrate metabolism - E74.8
  • Disorders of glucose transport, not elsewhere classified - E74.81
  • Glucose transporter protein type 1 deficiency - E74.810
  • Other disorders of glucose transport - E74.818
  • Disorders of glucose transport, unspecified - E74.819
  • Disorders of citrate metabolism - E74.82
  • SLC13A5 Citrate Transporter Disorder - E74.820
  • Other disorders of citrate metabolism - E74.829
  • Other specified disorders of carbohydrate metabolism - E74.89
  • Disorder of carbohydrate metabolism, unspecified - E74.9
  • GM2 gangliosidosis - E75.0
  • GM2 gangliosidosis, unspecified - E75.00
  • Sandhoff disease - E75.01
  • Tay-Sachs disease - E75.02
  • Other GM2 gangliosidosis - E75.09
  • Other and unspecified gangliosidosis - E75.1
  • Unspecified gangliosidosis - E75.10
  • Mucolipidosis IV - E75.11
  • Other gangliosidosis - E75.19
  • Other sphingolipidosis - E75.2
  • Fabry (-Anderson) disease - E75.21
  • Gaucher disease - E75.22
  • Krabbe disease - E75.23
  • Niemann-Pick disease - E75.24
  • Niemann-Pick disease type A - E75.240
  • Niemann-Pick disease type B - E75.241
  • Niemann-Pick disease type C - E75.242
  • Niemann-Pick disease type D - E75.243
  • Niemann-Pick disease type A/B - E75.244
  • Other Niemann-Pick disease - E75.248
  • Niemann-Pick disease, unspecified - E75.249
  • Metachromatic leukodystrophy - E75.25
  • Sulfatase deficiency - E75.26
  • Pelizaeus-Merzbacher disease - E75.27
  • Canavan disease - E75.28
  • Other sphingolipidosis - E75.29
  • Sphingolipidosis, unspecified - E75.3
  • Neuronal ceroid lipofuscinosis - E75.4
  • Other lipid storage disorders - E75.5
  • Lipid storage disorder, unspecified - E75.6
  • Mucopolysaccharidosis, type I - E76.0
  • Hurler's syndrome - E76.01
  • Hurler-Scheie syndrome - E76.02
  • Scheie's syndrome - E76.03
  • Mucopolysaccharidosis, type II - E76.1
  • Other mucopolysaccharidoses - E76.2
  • Morquio mucopolysaccharidoses - E76.21
  • Morquio A mucopolysaccharidoses - E76.210
  • Morquio B mucopolysaccharidoses - E76.211
  • Morquio mucopolysaccharidoses, unspecified - E76.219
  • Sanfilippo mucopolysaccharidoses - E76.22
  • Other mucopolysaccharidoses - E76.29
  • Mucopolysaccharidosis, unspecified - E76.3
  • Other disorders of glucosaminoglycan metabolism - E76.8
  • Glucosaminoglycan metabolism disorder, unspecified - E76.9
  • Defects in post-translational modification of lysosomal enzymes - E77.0
  • Defects in glycoprotein degradation - E77.1
  • Other disorders of glycoprotein metabolism - E77.8
  • Disorder of glycoprotein metabolism, unspecified - E77.9
  • Pure hypercholesterolemia - E78.0
  • Pure hypercholesterolemia, unspecified - E78.00
  • Familial hypercholesterolemia - E78.01
  • Pure hyperglyceridemia - E78.1
  • Mixed hyperlipidemia - E78.2
  • Hyperchylomicronemia - E78.3
  • Other hyperlipidemia - E78.4
  • Elevated Lipoprotein(a) - E78.41
  • Other hyperlipidemia - E78.49
  • Hyperlipidemia, unspecified - E78.5
  • Lipoprotein deficiency - E78.6
  • Disorders of bile acid and cholesterol metabolism - E78.7
  • Disorder of bile acid and cholesterol metabolism, unspecified - E78.70
  • Barth syndrome - E78.71
  • Smith-Lemli-Opitz syndrome - E78.72
  • Other disorders of bile acid and cholesterol metabolism - E78.79
  • Other disorders of lipoprotein metabolism - E78.8
  • Lipoid dermatoarthritis - E78.81
  • Other lipoprotein metabolism disorders - E78.89
  • Disorder of lipoprotein metabolism, unspecified - E78.9
  • Hyperuricemia without signs of inflammatory arthritis and tophaceous disease - E79.0
  • Lesch-Nyhan syndrome - E79.1
  • Myoadenylate deaminase deficiency - E79.2
  • Other disorders of purine and pyrimidine metabolism - E79.8
  • Aicardi-Goutières syndrome - E79.81
  • Hereditary xanthinuria - E79.82
  • Other specified disorders of purine and pyrimidine metabolism - E79.89
  • Disorder of purine and pyrimidine metabolism, unspecified - E79.9
  • Hereditary erythropoietic porphyria - E80.0
  • Porphyria cutanea tarda - E80.1
  • Other and unspecified porphyria - E80.2
  • Unspecified porphyria - E80.20
  • Acute intermittent (hepatic) porphyria - E80.21
  • Other porphyria - E80.29
  • Defects of catalase and peroxidase - E80.3
  • Gilbert syndrome - E80.4
  • Crigler-Najjar syndrome - E80.5
  • Other disorders of bilirubin metabolism - E80.6
  • Disorder of bilirubin metabolism, unspecified - E80.7