AutoICD API

E71.311

Billable

Medium chain acyl CoA dehydrogenase deficiency

Medium 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

  • MCAD 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 medium chain acyl coa dehydrogenase deficiency?

The ICD-10-CM code for medium chain acyl coa dehydrogenase deficiency is E71.311. The full clinical description is "Medium chain acyl CoA dehydrogenase deficiency". E71.311 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code E71.311 mean?

ICD-10-CM code E71.311 represents "Medium 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 E71.311 a billable code?

Yes, E71.311 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is E71.311 in?

E71.311 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).

What codes cannot be used with E71.311?

E71.311 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 E71.311 map to?

E71.311 maps to 2 SNOMED CT concepts: 128596003, 82319005. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for E71.311?

E71.311 is linked to 1 UMLS Concept Unique Identifier: C0220710. 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.