E71.310
BillableLong chain/very long chain acyl CoA dehydrogenase deficiency
Long chain/very long chain acyl CoA dehydrogenase deficiency
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 newbornP70-P74
- •androgen insensitivity syndromeE34.5
- •congenital adrenal hyperplasiaE25.0
- •hemolytic anemias attributable to enzyme disordersD55
- •Marfan syndromeQ87.4
- •5-alpha-reductase deficiencyE29.1
- •peroxisomal disordersE71.5
- •Refsum's diseaseG60.1
- •Schilder's diseaseG37.0
Excludes 2
Conditions not included here, but the patient may have both
Related Codes(5)
Also Known As / Clinical Terms(80)
SNOMED CT
- Acyl-CoA dehydrogenase deficiency82319005
- Acyl-coenzyme A dehydrogenase deficiency82319005
- Deficiency of acyl-CoA dehydrogenase82319005
- LCAD - Long chain acyl-CoA dehydrogenase deficiency237996001
- Long chain acyl-CoA dehydrogenase deficiency237996001
- Long chain acyl-coenzyme A dehydrogenase deficiency237996001
- VLCAD - Very long chain acyl-CoA dehydrogenase deficiency237997005
- Very long chain acyl-CoA dehydrogenase deficiency237997005
- Very long chain acyl-coenzyme A dehydrogenase deficiency237997005
- Combined deficiency of long chain 3-hydroxyacyl-CoA dehydrogenase and enoyl-CoA hydratase238000002
- Combined deficiency of long chain 3-hydroxyacyl-coenzyme A dehydrogenase and enoyl-coenzyme A hydratase238000002
UMLS
- ACADVLC3887523
- ACADVLDC3887523
- ACYL-CoA DEHYDROGENASE, VERY LONG-CHAIN, DEFICIENCY OFC3887523
- AcadvlC3887523
- Acyl-CoA Dehydrogenase, Very Long-Chain DeficiencyC3887523
- Acyl-CoA Dehydrogenase, Very Long-Chain, Deficiency ofC3887523
- Acyl-CoA dehydrogenase very long chain deficiencyC3887523
- Acyl-Coa Dehydrogenase Very Long Chain DeficiencyC3887523
- VLCADC3887523
- VLCAD - Very long chain acyl-CoA dehydrogenase deficiencyC3887523
- VLCAD DEFICIENCYC3887523
- VLCAD deficiencyC3887523
- VLCAD-CC3887523
- VLCAD-HC3887523
- Very Long-Chain Acyl Coenzyme A Dehydrogenase DeficiencyC3887523
- Very Long-Chain Acyl-CoA Dehydrogenase DeficiencyC3887523
- Very Long-Chain Acyl-Coenzyme A Dehydrogenase DeficiencyC3887523
- Very long chain acyl-CoA dehydrogenase deficiencyC3887523
- Very long chain acyl-coenzyme A dehydrogenase deficiencyC3887523
- Very long chain acyl-coenzyme A dehydrogenase deficiency (disorder)C3887523
- Very long-chain acyl coenzyme A dehydrogenase deficiencyC3887523
- Very long-chain acyl-CoA dehydrogenase deficiencyC3887523
- Very long-chain acyl-coenzyme A dehydrogenase deficiencyC3887523
- Vlcad-CC3887523
- Vlcad-HC3887523
- Acyl-CoA Dehydrogenase, Long-Chain DeficiencyC0220711
- Acyl-Coa Dehydrogenase, Long-Chain, Deficiency ofC0220711
- LCADC0220711
- LCAD - Long chain acyl-CoA dehydrogenase deficiencyC0220711
- LCAD deficiencyC0220711
- Long chain acyl-CoA dehydrogenase deficiencyC0220711
- Long chain acyl-coenzyme A dehydrogenase deficiencyC0220711
- Long chain acyl-coenzyme A dehydrogenase deficiency (disorder)C0220711
- Long-Chain Acyl-CoA Dehydrogenase DeficiencyC0220711
- Long-Chain Acyl-Coenzyme A Dehydrogenase DeficiencyC0220711
- Long-chain acyl-CoA dehydrogenase deficiencyC0220711
- Long-chain acyl-coenzyme A dehydrogenase deficiencyC0220711
- Long chain/very long chain acyl CoA dehydrogenase deficiencyC2874239
Clinical Terms
- Long-Chain Acyl-CoA Dehydrogenase Deficiency
- ACYL-CoA DEHYDROGENASE, VERY LONG-CHAIN, DEFICIENCY OF
- Combined deficiency of long chain 3-hydroxyacyl-coenzyme A dehydrogenase and enoyl-coenzyme A hydratase
- Acyl-CoA Dehydrogenase, Very Long-Chain Deficiency
- Very long chain acyl-CoA dehydrogenase deficiency
- Very Long-Chain Acyl Coenzyme A Dehydrogenase Deficiency
- VLCAD - Very long chain acyl-CoA dehydrogenase deficiency
- VLCAD-H
- Deficiency of acyl-CoA dehydrogenase
- Acyl-CoA dehydrogenase very long chain deficiency
- Very Long-Chain Acyl-CoA Dehydrogenase Deficiency
- Acadvl
- VLCAD DEFICIENCY
- Long chain acyl-coenzyme A dehydrogenase deficiency (disorder)
- LCAD - Long chain acyl-CoA dehydrogenase deficiency
- Acyl-Coa Dehydrogenase, Long-Chain, Deficiency of
- LCAD
- Very Long-Chain Acyl-Coenzyme A Dehydrogenase Deficiency
- Long chain acyl-CoA dehydrogenase deficiency
- VLCAD
- Long-Chain Acyl-Coenzyme A Dehydrogenase Deficiency
- Acyl-CoA dehydrogenase deficiency
- Long chain acyl-coenzyme A dehydrogenase deficiency
- Vlcad-C
- Combined deficiency of long chain 3-hydroxyacyl-CoA dehydrogenase and enoyl-CoA hydratase
- Acyl-CoA Dehydrogenase, Long-Chain Deficiency
- Acyl-coenzyme A dehydrogenase deficiency
- ACADVLD
- LCAD deficiency
- Very long chain acyl-coenzyme A dehydrogenase deficiency (disorder)
- Very long chain acyl-coenzyme A dehydrogenase deficiency
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.
How does E71.310 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like long chain/very long chain acyl coa dehydrogenase deficiency affect a person's functioning: body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.
What is the ICD-11 equivalent of E71.310?
There is no direct ICD-11 mapping available for E71.310 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.
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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.