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 97 of 1,952
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 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 Other disorders of amino-acid metabolism E72 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