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 77 of 1,952
Purine nucleoside phosphorylase [PNP] deficiency D81.5 Major histocompatibility complex class I deficiency D81.6 Major histocompatibility complex class II deficiency D81.7 Other combined immunodeficiencies D81.8 Biotin-dependent carboxylase deficiency D81.81 Biotinidase deficiency D81.810 Other biotin-dependent carboxylase deficiency D81.818 Biotin-dependent carboxylase deficiency, unspecified D81.819 Activated Phosphoinositide 3-kinase Delta Syndrome [APDS] D81.82 Other combined immunodeficiencies D81.89 Combined immunodeficiency, unspecified D81.9 Immunodeficiency associated with other major defects D82 Wiskott-Aldrich syndrome D82.0 Di George's syndrome D82.1 Immunodeficiency with short-limbed stature D82.2 Immunodeficiency following hereditary defective response to Epstein-Barr virus D82.3 Hyperimmunoglobulin E [IgE] syndrome D82.4 Immunodeficiency associated with other specified major defects D82.8 Immunodeficiency associated with major defect, unspecified D82.9 Common variable immunodeficiency D83 Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function D83.0 Common variable immunodeficiency with predominant immunoregulatory T-cell disorders D83.1 Common variable immunodeficiency with autoantibodies to B- or T-cells D83.2 Other common variable immunodeficiencies D83.8 Common variable immunodeficiency, unspecified D83.9 Other immunodeficiencies D84 Lymphocyte function antigen-1 [LFA-1] defect D84.0 Defects in the complement system D84.1 Other specified immunodeficiencies D84.8 Immunodeficiency due to conditions classified elsewhere D84.81 Immunodeficiency due to drugs and external causes D84.82 Immunodeficiency due to drugs D84.821 Immunodeficiency due to external causes D84.822 Other immunodeficiencies D84.89 Immunodeficiency, unspecified D84.9 Sarcoidosis D86 Sarcoidosis of lung D86.0 Sarcoidosis of lymph nodes D86.1 Sarcoidosis of lung with sarcoidosis of lymph nodes D86.2 Sarcoidosis of skin D86.3 Sarcoidosis of other sites D86.8 Sarcoid meningitis D86.81 Multiple cranial nerve palsies in sarcoidosis D86.82 Sarcoid iridocyclitis D86.83 Sarcoid pyelonephritis D86.84 Sarcoid myocarditis D86.85 Sarcoid arthropathy D86.86 Sarcoid myositis D86.87 Sarcoidosis of other sites D86.89 Sarcoidosis, unspecified D86.9