AutoICD API

E71.310

Billable

Long chain/very long chain acyl CoA dehydrogenase deficiency

Long chain/very long chain acyl CoA dehydrogenase deficiency

Status

Billable / Specific

Block

E70-E88

Parent Code

E71.31

Coding Notes

Inclusion Terms

Alternative clinical terms for this condition

  • LCAD deficiency
  • VLCAD deficiency

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)
  • peroxisomal disorders (E71.5)
  • Refsum's disease (G60.1)
  • Schilder's disease (G37.0)

Excludes 2

Conditions not included here, but the patient may have both

  • Ehlers-Danlos syndromes (Q79.6-)
  • carnitine deficiency due to inborn error of metabolism (E71.42)

Also Known As / Clinical Terms

SNOMED CT

UMLS

Frequently Asked Questions

What is the ICD-10 code for long chain/very long chain acyl coa dehydrogenase deficiency?

The ICD-10-CM code for long chain/very long chain acyl coa dehydrogenase deficiency is E71.310. The full clinical description is "Long chain/very long chain acyl CoA dehydrogenase deficiency". E71.310 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code E71.310 mean?

ICD-10-CM code E71.310 represents "Long chain/very long chain acyl CoA dehydrogenase deficiency". 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 E71.310 a billable code?

Yes, E71.310 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is E71.310 in?

E71.310 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).

What codes cannot be used with E71.310?

E71.310 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 6 more.

What SNOMED CT codes does E71.310 map to?

E71.310 maps to 4 SNOMED CT concepts: 82319005, 238000002, 237996001, 237997005. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for E71.310?

E71.310 is linked to 3 UMLS Concept Unique Identifiers: C3887523, C0220711, C2874239. 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.