MCMedicalCodingSoftware
E71.42

E71.42: Carnitine deficiency due to inborn errors of metabolism

Billable / specific codeICD-10-CM

E71.42 is a billable, specific ICD-10-CM code for carnitine deficiency due to inborn errors of metabolism. It is valid for submission on a claim.

Check E71.42 with the rest of the claim: free scrubber

Code also

Both codes may be needed to describe the encounter fully. Sequencing depends on the reason for the visit.

  • associated inborn error or metabolism

Excludes1 inherited from the categories above E71.42

A category’s note binds every code beneath it.

Written on E71.4: Disorders of carnitine metabolism

  • Muscle carnitine palmitoyltransferase deficiency (E71.314)

Other codes that can never be billed with E71.42

Their own Excludes1 notes name this code, so the conflict is not listed above.

  • E71.511Neonatal adrenoleukodystrophy

Risk adjustment

No CMS-HCC V28 category: this code does not change a RAF score.

Medicare coverage

E71.42 is named in 3 Medicare coverage policies: 3 listing it as supporting medical necessity. Which one applies depends on your Medicare contractor.

  • A54095Billing and Coding: Nerve Conduction Studies and Electromyography
  • A56416Billing and Coding: Assays for Vitamins and Metabolic Function
  • A57123Billing and Coding: Nerve Conduction Studies and Electromyography

Alphabetic index entries that lead here

  • Deficiency, deficient›carnitine›due to›inborn errors of metabolism

Code history

Unchanged in every release from FY2024 to FY2027.

Other codes under E71.4

ICD-10-CMFY2027· effective October 1, 2026

Loaded directly from the CMS/NCHS ICD-10-CM public-domain release: see data sources and our editorial policy. If this page disagrees with the CMS tabular list, this page is wrong. Reference information for professional coders; not medical or billing advice.