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 74 of 1,952
Von Willebrand disease, type 3 D68.03 Acquired von Willebrand disease D68.04 Other von Willebrand disease D68.09 Hereditary factor XI deficiency D68.1 Hereditary deficiency of other clotting factors D68.2 Hemorrhagic disorder due to circulating anticoagulants D68.3 Hemorrhagic disorder due to intrns circ anticoag,antib,inhib Hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors D68.31 Acquired hemophilia D68.311 Antiphospholipid antibody with hemorrhagic disorder D68.312 Other hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors D68.318 Hemorrhagic disorder due to extrinsic circulating anticoagulants D68.32 Acquired coagulation factor deficiency D68.4 Primary thrombophilia D68.5 Activated protein C resistance D68.51 Prothrombin gene mutation D68.52 Other primary thrombophilia D68.59 Other thrombophilia D68.6 Antiphospholipid syndrome D68.61 Lupus anticoagulant syndrome D68.62 Other thrombophilia D68.69 Other specified coagulation defects D68.8 Coagulation defect, unspecified D68.9 Purpura and other hemorrhagic conditions D69 Allergic purpura D69.0 Qualitative platelet defects D69.1 Other nonthrombocytopenic purpura D69.2 Immune thrombocytopenic purpura D69.3 Other primary thrombocytopenia D69.4 Evans syndrome D69.41 Congenital and hereditary thrombocytopenia purpura D69.42 Other primary thrombocytopenia D69.49 Secondary thrombocytopenia D69.5 Posttransfusion purpura D69.51 Other secondary thrombocytopenia D69.59 Thrombocytopenia, unspecified D69.6 Other specified hemorrhagic conditions D69.8 Hemorrhagic condition, unspecified D69.9 Neutropenia D70 Congenital agranulocytosis D70.0 Agranulocytosis secondary to cancer chemotherapy D70.1 Other drug-induced agranulocytosis D70.2 Neutropenia due to infection D70.3 Cyclic neutropenia D70.4 Other neutropenia D70.8 Neutropenia, unspecified D70.9 Functional disorders of polymorphonuclear neutrophils D71 Other disorders of white blood cells D72 Genetic anomalies of leukocytes D72.0 Eosinophilia D72.1 Eosinophilia, unspecified D72.10