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