E71.42

Billable

Carnitine deficiency due to inborn errors of metabolism

Carnitine deficiency due to inborn errors of metabolism

Status

Billable / Specific

Block

E70-E88

Parent Code

E71.4

Coding Notes

Excludes 1

Codes that cannot be used together with this code (mutual exclusion)

  • transitory endocrine and metabolic disorders specific to newborn (P70-P74)
  • androgen insensitivity syndrome (E34.5-)
  • congenital adrenal hyperplasia (E25.0)
  • hemolytic anemias attributable to enzyme disorders (D55.-)
  • Marfan syndrome (Q87.4-)
  • 5-alpha-reductase deficiency (E29.1)
  • Muscle carnitine palmitoyltransferase deficiency (E71.314)

Excludes 2

Conditions not included here, but the patient may have both

  • Ehlers-Danlos syndromes (Q79.6-)

Code Also

A second code may be required; sequencing depends on circumstances

  • associated inborn error or metabolism

Also Known As / Clinical Terms

Frequently Asked Questions

What is the ICD-10 code for carnitine deficiency due to inborn errors of metabolism?

The ICD-10-CM code for carnitine deficiency due to inborn errors of metabolism is E71.42. The full clinical description is "Carnitine deficiency due to inborn errors of metabolism". E71.42 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code E71.42 mean?

ICD-10-CM code E71.42 represents "Carnitine deficiency due to inborn errors of metabolism". It is classified under Chapter 4: Endocrine, Nutritional and Metabolic Diseases and is a billable/specific code that can be used on a claim.

Is E71.42 a billable code?

Yes, E71.42 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is E71.42 in?

E71.42 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).

What codes cannot be used with E71.42?

E71.42 has Excludes1 notes indicating codes that cannot be used together with it, including: transitory endocrine and metabolic disorders specific to newborn (P70-P74); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); and 4 more.

What SNOMED CT codes does E71.42 map to?

E71.42 maps to 4 SNOMED CT concepts: 82994006, 421784001, 55341000119107, 1366322006. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for E71.42?

E71.42 is linked to 1 UMLS Concept Unique Identifier: C3875374. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.