| ICD-10-CM-2023 > E00-E89 > E70-E88 > E88 |
E70-E88 | Metabolic disorders | |
Excl1.: | androgen insensitivity syndrome (E34.5-) congenital adrenal hyperplasia (E25.0) hemolytic anemias attributable to enzyme disorders (D55.-) Marfan's syndrome (Q87.4) 5-alpha-reductase deficiency (E29.1) | |
Excl2.: | Ehlers-Danlos syndromes (Q79.6-) | |
E88 | Other and unspecified metabolic disorders | |
Use add'l | codes for associated conditions | |
Excl1.: | histiocytosis X (chronic) (C96.6) | |
E88.0 | Disorders of plasma-protein metabolism, not elsewhere classified | |
Excl1.: | monoclonal gammopathy (of undetermined significance) (D47.2) polyclonal hypergammaglobulinemia (D89.0) Waldenström macroglobulinemia (C88.0) | |
Excl2.: | disorder of lipoprotein metabolism (E78.-) | |
E88.01 | Alpha-1-antitrypsin deficiency | |
Info: | AAT deficiency | |
E88.02 | Plasminogen deficiency | |
Info: | Dysplasminogenemia Hypoplasminogenemia Type 1 plasminogen deficiency Type 2 plasminogen deficiency | |
Use add'l | , if applicable, ligneous conjunctivitis (H10.51) | |
Use add'l | code for associated findings, such as: hydrocephalus (G91.4) otitis media (H67.-) respiratory disorder related to plasminogen deficiency (J99) | |
E88.09 | Other disorders of plasma-protein metabolism, not elsewhere classified | |
Info: | Bisalbuminemia | |
E88.1 | Lipodystrophy, not elsewhere classified | |
Info: | Lipodystrophy NOS | |
Excl1.: | Whipple's disease (K90.81) | |
E88.2 | Lipomatosis, not elsewhere classified | |
Info: | Lipomatosis NOS Lipomatosis (Check) dolorosa [Dercum] | |
E88.3 | Tumor lysis syndrome | |
Info: | Tumor lysis syndrome (spontaneous) Tumor lysis syndrome following antineoplastic drug chemotherapy | |
Use add'l | code for adverse effect, if applicable, to identify drug (T45.1X5) | |
E88.4 | Mitochondrial metabolism disorders | |
Excl1.: | disorders of pyruvate metabolism (E74.4) Kearns-Sayre syndrome (H49.81) Leber's disease (H47.22) Leigh's encephalopathy (G31.82) Mitochondrial myopathy, NEC (G71.3) Reye's syndrome (G93.7) | |
E88.40 | Mitochondrial metabolism disorder, unspecified | |
E88.41 | MELAS syndrome | |
Info: | Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes | |
E88.42 | MERRF syndrome | |
Info: | Myoclonic epilepsy associated with ragged-red fibers | |
Use add'l | progressive myoclonic epilepsy (G40.3-) | |
E88.49 | Other mitochondrial metabolism disorders | |
E88.8 | Other specified metabolic disorders | |
E88.81 | Metabolic syndrome | |
Info: | Dysmetabolic syndrome X | |
Use add'l | codes for associated manifestations, such as: obesity (E66.-) | |
E88.89 | Other specified metabolic disorders | |
Info: | Launois-Bensaude adenolipomatosis | |
Excl1.: | adult pulmonary Langerhans cell histiocytosis (J84.82) | |
E88.9 | Metabolic disorder, unspecified | |
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