Billable/Specific ICD-10-CM Codes - Page 37
There are 35,750 ICD-10-CM codes which are billable/specific and can be used to indicate a diagnosis for reimbursement purposes as there are no codes with a greater level of specificity under each code.
- E72.59 - Other disorders of glycine metabolism
- E72.81 - Disorders of gamma aminobutyric acid metabolism
- E72.89 - Other specified disorders of amino-acid metabolism
- E72.9 - Disorder of amino-acid metabolism, unspecified
- E73.0 - Congenital lactase deficiency
- E73.1 - Secondary lactase deficiency
- E73.8 - Other lactose intolerance
- E73.9 - Lactose intolerance, unspecified
- E74.00 - Glycogen storage disease, unspecified
- E74.01 - von Gierke disease
- E74.02 - Pompe disease
- E74.03 - Cori disease
- E74.04 - McArdle disease
- E74.05 - Lysosome-associated membrane protein 2 [LAMP2] deficiency
- E74.09 - Other glycogen storage disease
- E74.10 - Disorder of fructose metabolism, unspecified
- E74.11 - Essential fructosuria
- E74.12 - Hereditary fructose intolerance
- E74.19 - Other disorders of fructose metabolism
- E74.20 - Disorders of galactose metabolism, unspecified
- E74.21 - Galactosemia
- E74.29 - Other disorders of galactose metabolism
- E74.31 - Sucrase-isomaltase deficiency
- E74.39 - Other disorders of intestinal carbohydrate absorption
- E74.4 - Disorders of pyruvate metabolism and gluconeogenesis
- E74.810 - Glucose transporter protein type 1 deficiency
- E74.818 - Other disorders of glucose transport
- E74.819 - Disorders of glucose transport, unspecified
- E74.820 - SLC13A5 Citrate Transporter Disorder
- E74.829 - Other disorders of citrate metabolism
- E74.89 - Other specified disorders of carbohydrate metabolism
- E74.9 - Disorder of carbohydrate metabolism, unspecified
- E75.00 - GM2 gangliosidosis, unspecified
- E75.01 - Sandhoff disease
- E75.02 - Tay-Sachs disease
- E75.09 - Other GM2 gangliosidosis
- E75.10 - Unspecified gangliosidosis
- E75.11 - Mucolipidosis IV
- E75.19 - Other gangliosidosis
- E75.21 - Fabry (-Anderson) disease
- E75.22 - Gaucher disease
- E75.23 - Krabbe disease
- E75.240 - Niemann-Pick disease type A
- E75.241 - Niemann-Pick disease type B
- E75.242 - Niemann-Pick disease type C
- E75.243 - Niemann-Pick disease type D
- E75.244 - Niemann-Pick disease type A/B
- E75.248 - Other Niemann-Pick disease
- E75.249 - Niemann-Pick disease, unspecified
- E75.25 - Metachromatic leukodystrophy
- E75.26 - Sulfatase deficiency
- E75.27 - Pelizaeus-Merzbacher disease
- E75.28 - Canavan disease
- E75.29 - Other sphingolipidosis
- E75.3 - Sphingolipidosis, unspecified
- E75.4 - Neuronal ceroid lipofuscinosis
- E75.5 - Other lipid storage disorders
- E75.6 - Lipid storage disorder, unspecified
- E76.01 - Hurler's syndrome
- E76.02 - Hurler-Scheie syndrome
- E76.03 - Scheie's syndrome
- E76.1 - Mucopolysaccharidosis, type II
- E76.210 - Morquio A mucopolysaccharidoses
- E76.211 - Morquio B mucopolysaccharidoses
- E76.219 - Morquio mucopolysaccharidoses, unspecified
- E76.22 - Sanfilippo mucopolysaccharidoses
- E76.29 - Other mucopolysaccharidoses
- E76.3 - Mucopolysaccharidosis, unspecified
- E76.8 - Other disorders of glucosaminoglycan metabolism
- E76.9 - Glucosaminoglycan metabolism disorder, unspecified
- E77.0 - Defects in post-translational modification of lysosomal enzymes
- E77.1 - Defects in glycoprotein degradation
- E77.8 - Other disorders of glycoprotein metabolism
- E77.9 - Disorder of glycoprotein metabolism, unspecified
- E78.00 - Pure hypercholesterolemia, unspecified
- E78.01 - Familial hypercholesterolemia
- E78.1 - Pure hyperglyceridemia
- E78.2 - Mixed hyperlipidemia
- E78.3 - Hyperchylomicronemia
- E78.41 - Elevated Lipoprotein(a)
- E78.49 - Other hyperlipidemia
- E78.5 - Hyperlipidemia, unspecified
- E78.6 - Lipoprotein deficiency
- E78.70 - Disorder of bile acid and cholesterol metabolism, unspecified
- E78.71 - Barth syndrome
- E78.72 - Smith-Lemli-Opitz syndrome
- E78.79 - Other disorders of bile acid and cholesterol metabolism
- E78.81 - Lipoid dermatoarthritis
- E78.89 - Other lipoprotein metabolism disorders
- E78.9 - Disorder of lipoprotein metabolism, unspecified
- E79.0 - Hyperuricemia without signs of inflammatory arthritis and tophaceous disease
- E79.1 - Lesch-Nyhan syndrome
- E79.2 - Myoadenylate deaminase deficiency
- E79.81 - Aicardi-Goutières syndrome
- E79.82 - Hereditary xanthinuria
- E79.89 - Other specified disorders of purine and pyrimidine metabolism
- E79.9 - Disorder of purine and pyrimidine metabolism, unspecified
- E80.0 - Hereditary erythropoietic porphyria
- E80.1 - Porphyria cutanea tarda
- E80.20 - Unspecified porphyria