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 78 of 1,952
Other disorders involving the immune mechanism, not elsewhere classified D89 Polyclonal hypergammaglobulinemia D89.0 Cryoglobulinemia D89.1 Hypergammaglobulinemia, unspecified D89.2 Immune reconstitution syndrome D89.3 Mast cell activation syndrome and related disorders D89.4 Mast cell activation, unspecified D89.40 Monoclonal mast cell activation syndrome D89.41 Idiopathic mast cell activation syndrome D89.42 Secondary mast cell activation D89.43 Hereditary alpha tryptasemia D89.44 Other mast cell activation disorder D89.49 Other specified disorders involving the immune mechanism, not elsewhere classified D89.8 Graft-versus-host disease D89.81 Acute graft-versus-host disease D89.810 Chronic graft-versus-host disease D89.811 Acute on chronic graft-versus-host disease D89.812 Graft-versus-host disease, unspecified D89.813 Autoimmune lymphoproliferative syndrome [ALPS] D89.82 Cytokine release syndrome D89.83 Cytokine release syndrome, grade 1 D89.831 Cytokine release syndrome, grade 2 D89.832 Cytokine release syndrome, grade 3 D89.833 Cytokine release syndrome, grade 4 D89.834 Cytokine release syndrome, grade 5 D89.835 Cytokine release syndrome, grade unspecified D89.839 IgG4-related disease D89.84 Other specified disorders involving the immune mechanism, not elsewhere classified D89.89 Disorder involving the immune mechanism, unspecified D89.9 Congenital iodine-deficiency syndrome E00 Congenital iodine-deficiency syndrome, neurological type E00.0 Congenital iodine-deficiency syndrome, myxedematous type E00.1 Congenital iodine-deficiency syndrome, mixed type E00.2 Congenital iodine-deficiency syndrome, unspecified E00.9 Iodine-deficiency related thyroid disorders and allied conditions E01 Iodine-deficiency related diffuse (endemic) goiter E01.0 Iodine-deficiency related multinodular (endemic) goiter E01.1 Iodine-deficiency related (endemic) goiter, unspecified E01.2 Oth iodine-deficiency related thyroid disord and allied cond Other iodine-deficiency related thyroid disorders and allied conditions E01.8 Subclinical iodine-deficiency hypothyroidism E02 Other hypothyroidism E03 Congenital hypothyroidism with diffuse goiter E03.0 Congenital hypothyroidism without goiter E03.1 Hypothyroidism due to medicaments and other exogenous substances E03.2 Postinfectious hypothyroidism E03.3 Atrophy of thyroid (acquired) E03.4 Myxedema coma E03.5 Other specified hypothyroidism E03.8 Hypothyroidism, unspecified E03.9 Other nontoxic goiter E04