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 138 of 1,952
Hereditary motor and sensory neuropathy G60.0 Refsum's disease G60.1 Neuropathy in association with hereditary ataxia G60.2 Idiopathic progressive neuropathy G60.3 Other hereditary and idiopathic neuropathies G60.8 Hereditary and idiopathic neuropathy, unspecified G60.9 Inflammatory polyneuropathy G61 Guillain-Barre syndrome G61.0 Serum neuropathy G61.1 Other inflammatory polyneuropathies G61.8 Chronic inflammatory demyelinating polyneuritis G61.81 Multifocal motor neuropathy G61.82 Other inflammatory polyneuropathies G61.89 Inflammatory polyneuropathy, unspecified G61.9 Other and unspecified polyneuropathies G62 Drug-induced polyneuropathy G62.0 Alcoholic polyneuropathy G62.1 Polyneuropathy due to other toxic agents G62.2 Other specified polyneuropathies G62.8 Critical illness polyneuropathy G62.81 Radiation-induced polyneuropathy G62.82 Other specified polyneuropathies G62.89 Polyneuropathy, unspecified G62.9 Polyneuropathy in diseases classified elsewhere G63 Other disorders of peripheral nervous system G64 Sequelae of inflammatory and toxic polyneuropathies G65 Sequelae of Guillain-Barre syndrome G65.0 Sequelae of other inflammatory polyneuropathy G65.1 Sequelae of toxic polyneuropathy G65.2 Myasthenia gravis and other myoneural disorders G70 Myasthenia gravis G70.0 Myasthenia gravis without (acute) exacerbation G70.00 Myasthenia gravis with (acute) exacerbation G70.01 Toxic myoneural disorders G70.1 Congenital and developmental myasthenia G70.2 Other specified myoneural disorders G70.8 Lambert-Eaton syndrome, unspecified G70.80 Lambert-Eaton syndrome in disease classified elsewhere G70.81 Other specified myoneural disorders G70.89 Myoneural disorder, unspecified G70.9 Primary disorders of muscles G71 Muscular dystrophy G71.0 Muscular dystrophy, unspecified G71.00 Duchenne or Becker muscular dystrophy G71.01 Facioscapulohumeral muscular dystrophy G71.02 Limb girdle muscular dystrophies G71.03 Autosomal dominant limb girdle muscular dystrophy G71.031 Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction G71.032 Limb girdle muscular dystrophy due to dysferlin dysfunction G71.033 Limb girdle muscular dystrophy due to sarcoglycan dysfunction G71.034