Index to Diseases and Injuries
Disorder › metabolism NOS
Index code:E88.9
- amino-acid E72.9
- aromatic E70.9
- albinism — see Albinism
- histidine E70.40
- histidinemia E70.41
- other specified E70.49
- hyperphenylalaninemia E70.1
- classical phenylketonuria E70.0
- other specified E70.89
- tryptophan E70.5
- tyrosine E70.20
- hypertyrosinemia E70.21
- other specified E70.29
- branched chain E71.2
- 3-methylglutaconic aciduria E71.111
- hyperleucine-isoleucinemia E71.19
- hypervalinemia E71.19
- isovaleric acidemia E71.110
- maple syrup urine disease E71.0
- methylmalonic acidemia E71.120
- organic aciduria NEC E71.118
- other specified E71.19
- propionate NEC E71.128
- propionic acidemia E71.121
- glycine E72.50
- d-glycericacidemia E72.59
- hyperhydroxyprolinemia E72.59
- hyperoxaluria R82.992
- primary E72.53
- hyperprolinemia E72.59
- non-ketotic hyperglycinemia E72.51
- other specified E72.59
- sarcosinemia E72.59
- trimethylaminuria E72.52
- hydroxylysine E72.3
- lysine E72.3
- ornithine E72.4
- other specified E72.89
- beta-amino acid E72.89
- gamma-glutamyl cycle E72.89
- straight-chain E72.89
- sulfur-bearing E72.10
- homocystinuria E72.11
- methylenetetrahydrofolate reductase deficiency E72.12
- other specified E72.19
- bile acid and cholesterol metabolism E78.70
- bilirubin E80.7
- specified NEC E80.6
- calcium E83.50
- hypercalcemia E83.52
- hypocalcemia E83.51
- other specified E83.59
- carbohydrate E74.9
- specified NEC E74.89
- cholesterol and bile acid metabolism E78.70
- citrate NEC E74.829
- congenital E88.9
- copper E83.00
- Wilson's disease E83.01
- specified type NEC E83.09
- cystinuria E72.01
- fructose E74.10
- galactose E74.20
- glucosaminoglycan E76.9
- mucopolysaccharidosis — see Mucopolysaccharidosis
- specified NEC E76.8
- glutamine E72.89
- glycine E72.50
- glycogen storage (hepatorenal) E74.09
- glycoprotein E77.9
- specified NEC E77.8
- glycosaminoglycan E76.9
- specified NEC E76.8
- in labor and delivery O75.89
- iron E83.10
- isoleucine E71.19
- leucine E71.19
- lipoid E78.9
- lipoprotein E78.9
- specified NEC E78.89
- magnesium E83.40
- hypermagnesemia E83.41
- hypomagnesemia E83.42
- other specified E83.49
- mineral E83.9
- specified NEC E83.89
- mitochondrial E88.40
- aminoacyl-tRNA synthetase E88.43
- ARS2-related E88.43
- MELAS syndrome E88.41
- MERRF syndrome (myoclonic epilepsy associated with ragged-red fibers) E88.42
- other specified E88.49
- tRNA synthetases E88.43
- ornithine E72.4
- phosphatases E83.30
- phosphorus E83.30
- acid phosphatase deficiency E83.39
- hypophosphatasia E83.39
- hypophosphatemia E83.39
- familial E83.31
- other specified E83.39
- pseudovitamin D deficiency E83.32
- plasma protein NEC E88.09
- porphyrin — see Porphyria
- postprocedural E89.89
- specified NEC E89.89
- purine E79.9
- specified NEC E79.89
- pyrimidine E79.9
- specified NEC E79.89
- pyruvate E74.4
- serine E72.89
- sodium E87.8
- specified NEC E88.89
- threonine E72.89
- valine E71.19
- zinc E83.2
Use the index to find a code, then confirm it in the Tabular List before assigning it. A code ending in a dash is incomplete, and a code in [brackets] is a manifestation code reported after the underlying condition. Search the whole index.
Frequently asked questions
What is the ICD-10-CM code for Disorder › metabolism NOS?
The ICD-10-CM Alphabetic Index directs "Disorder › metabolism NOS" to E88.9. Subterms below it may lead to a more specific code. Always confirm the code in the Tabular List before assigning it.
ICD-10-CM Index to Diseases and Injuries maintained by CDC/NCHS (public domain), from the CMS FY2027 release.