ICD-10-CM · Chapter 4 · E00–E89
E71.518
Other disorders of peroxisome biogenesis
Endocrine, nutritional and metabolic diseases
Quick facts
- Code
- E71.518
- Type
- Billable code
- ICD-10-CM chapter
- Chapter 4 — Endocrine, nutritional and metabolic diseases
- Category
- E71 — Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism
- Specificity
- 6 characters
How coders use this code
ICD-10-CM E71.518 is a billable, fully specified code, so it can be reported directly on a claim to document a diagnosis of other disorders of peroxisome biogenesis. Coders assign it when the chart documentation supports this level of detail, always matching to the most specific code available and verifying against the chapter-specific guidelines published annually by NCHS/CMS.
Related codes in E71
- E71Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism
- E71.0Maple-syrup-urine disease
- E71.1Other disorders of branched-chain amino-acid metabolism
- E71.11Branched-chain organic acidurias
- E71.110Isovaleric acidemia
- E71.1113-methylglutaconic aciduria
- E71.118Other branched-chain organic acidurias
- E71.12Disorders of propionate metabolism
- E71.120Methylmalonic acidemia
- E71.121Propionic acidemia
- E71.128Other disorders of propionate metabolism
- E71.19Other disorders of branched-chain amino-acid metabolism
- E71.2Disorder of branched-chain amino-acid metabolism, unspecified
- E71.3Disorders of fatty-acid metabolism
- E71.30Disorder of fatty-acid metabolism, unspecified
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