ICD-10-CM codes
The diagnosis classification on lab requisitions and clinical records. Every condition on this site is anchored to an ICD-10-CM code.
By chapter
22 chapters Certain infectious and parasitic diseases · A00–B99 1,307 Neoplasms · C00–D49 2,174 Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism · D50–D89 398 Endocrine, nutritional and metabolic diseases · E00–E89 1,242 Mental, behavioral and neurodevelopmental disorders · F01–F99 1,112 Diseases of the nervous system · G00–G99 920 Diseases of the eye and adnexa · H00–H59 3,447 Diseases of the ear and mastoid process · H60–H95 871 Diseases of the circulatory system · I00–I99 1,793 Diseases of the respiratory system · J00–J99 471 Diseases of the digestive system · K00–K95 1,109 Diseases of the skin and subcutaneous tissue · L00–L99 1,072 Diseases of the musculoskeletal system and connective tissue · M00–M99 8,673 Diseases of the genitourinary system · N00–N99 1,037 Pregnancy, childbirth and the puerperium · O00–O9A 3,023 Certain conditions originating in the perinatal period · P00–P96 565 Congenital malformations, deformations and chromosomal abnormalities · Q00–Q99 1,055 Symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified · R00–R99 938 Injury, poisoning and certain other consequences of external causes · S00–T88 53,983 Codes for special purposes · U00–U85 5 External causes of morbidity · V00–Y99 10,573 Factors influencing health status and contact with health services · Z00–Z99 1,816
All codes
97,584 codes · page 98 of 1,952
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 Lactose intolerance E73 Congenital lactase deficiency E73.0 Secondary lactase deficiency E73.1 Other lactose intolerance E73.8 Lactose intolerance, unspecified E73.9 Other disorders of carbohydrate metabolism E74 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 Other disorders of intestinal carbohydrate absorption E74.39