E71.312
BillableShort chain acyl CoA dehydrogenase deficiency
Short chain acyl CoA dehydrogenase deficiency
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- SCAD 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(81)
SNOMED CT
- Acyl-CoA dehydrogenase deficiency82319005
- Acyl-coenzyme A dehydrogenase deficiency82319005
- Deficiency of acyl-CoA dehydrogenase82319005
- Butyryl-CoA dehydrogenase deficiency124166007
- Deficiency of butyryl dehydrogenase124166007
- Deficiency of butyryl-CoA dehydrogenase124166007
- Deficiency of unsaturated acyl-CoA reductase124166007
- Deficiency of dehydrogenase124226002
- Short chain 3-hydroxyacyl-CoA dehydrogenase deficiency237998000
- Short chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency237998000
- ACADS - short chain acyl-coenzyme A dehydrogenase deficiency787412002
- SCAD - short chain acyl-CoA dehydrogenase deficiency787412002
- Short chain acyl-CoA dehydrogenase deficiency787412002
- Short chain acyl-coenzyme A dehydrogenase deficiency787412002
- 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency801000124108
UMLS
- ACADS - short chain acyl-coenzyme A dehydrogenase deficiencyC0342783
- ACADS DEFICIENCYC0342783
- ACADS deficiencyC0342783
- ACADSDC0342783
- ACYL-CoA DEHYDROGENASE, SHORT-CHAIN, DEFICIENCY OFC0342783
- Acads DeficiencyC0342783
- Acyl-CoA Dehydrogenase, Short-Chain DeficiencyC0342783
- Acyl-Coa Dehydrogenase, Short-Chain, Deficiency OfC0342783
- Butyryl-CoA Dehydrogenase DeficiencyC0342783
- Butyryl-CoA dehydrogenase deficiencyC0342783
- Deficiency of Butyryl-Coa DehydrogenaseC0342783
- Deficiency of butyryl dehydrogenaseC0342783
- Deficiency of butyryl-CoA dehydrogenaseC0342783
- Deficiency of butyryl-CoA dehydrogenase (disorder)C0342783
- Deficiency of unsaturated acyl-CoA reductaseC0342783
- LIPID-STORAGE MYOPATHY SECONDARY TO SHORT-CHAIN ACYL-CoA DEHYDROGENASE DEFICIENCYC0342783
- Lipid-Storage Myopathy Secondary to Short-Chain Acyl-Coa Dehydrogenase DeficiencyC0342783
- Lipid-storage myopathy secondary to short-chain acyl-coa dehydrogenase deficiencyC0342783
- SCADC0342783
- SCAD - short chain acyl-CoA dehydrogenase deficiencyC0342783
- SCAD DEFICIENCYC0342783
- SCAD deficiencyC0342783
- SCADH DEFICIENCYC0342783
- SCADH deficiencyC0342783
- Scad DeficiencyC0342783
- Scadh DeficiencyC0342783
- Short chain Acyl CoA dehydrogenase deficiencyC0342783
- Short chain acyl CoA dehydrogenase deficiencyC0342783
- Short chain acyl-CoA dehydrogenase deficiencyC0342783
- Short chain acyl-coenzyme A dehydrogenase deficiencyC0342783
- Short chain acyl-coenzyme A dehydrogenase deficiency (disorder)C0342783
- Short-Chain Acyl-CoA Dehydrogenase Deficiency (SCAD)C0342783
- Short-Chain Acyl-Coa Dehydrogenase DeficiencyC0342783
- Short-Chain Acyl-Coenzyme A Dehydrogenase DeficiencyC0342783
- Short-Chain Acyl-Coenzyme A Dehydrogenase Deficiency (SCAD)C0342783
- Short-chain acyl-CoA dehydrogenase deficiencyC0342783
- Short-chain acyl-coenzyme A dehydrogenase deficiencyC0342783
Clinical Terms
- Acyl-CoA Dehydrogenase, Short-Chain Deficiency
- Scadh Deficiency
- Short-Chain Acyl-CoA Dehydrogenase Deficiency (SCAD)
- Short-Chain Acyl-Coenzyme A Dehydrogenase Deficiency (SCAD)
- Short chain acyl-coenzyme A dehydrogenase deficiency (disorder)
- LIPID-STORAGE MYOPATHY SECONDARY TO SHORT-CHAIN ACYL-CoA DEHYDROGENASE DEFICIENCY
- SCAD DEFICIENCY
- Deficiency of butyryl-CoA dehydrogenase
- ACADS DEFICIENCY
- Deficiency of acyl-CoA dehydrogenase
- Short-chain acyl-coenzyme A dehydrogenase deficiency
- Acyl-Coa Dehydrogenase, Short-Chain, Deficiency Of
- Deficiency of butyryl-CoA dehydrogenase (disorder)
- ACADS - short chain acyl-coenzyme A dehydrogenase deficiency
- ACADSD
- Short chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
- 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency
- Acyl-CoA dehydrogenase deficiency
- Butyryl-CoA dehydrogenase deficiency
- Deficiency of unsaturated acyl-CoA reductase
- Short-Chain Acyl-Coa Dehydrogenase Deficiency
- Short chain acyl-coenzyme A dehydrogenase deficiency
- Short chain 3-hydroxyacyl-CoA dehydrogenase deficiency
- Deficiency of butyryl dehydrogenase
- Acyl-coenzyme A dehydrogenase deficiency
- SCAD - short chain acyl-CoA dehydrogenase deficiency
- Deficiency of dehydrogenase
- Short chain acyl-CoA dehydrogenase deficiency
- SCAD
Frequently Asked Questions
What is the ICD-10 code for short chain acyl coa dehydrogenase deficiency?
The ICD-10-CM code for short chain acyl coa dehydrogenase deficiency is E71.312. The full clinical description is "Short chain acyl CoA dehydrogenase deficiency". E71.312 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E71.312 mean?
ICD-10-CM code E71.312 represents “Short 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 E71.312 a billable code?
Yes, E71.312 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E71.312 in?
E71.312 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E71.312?
E71.312 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 E71.312 map to?
E71.312 maps to 6 SNOMED CT concepts: 801000124108, 787412002, 82319005, 124166007, 124226002, and 1 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E71.312?
E71.312 is linked to 1 UMLS Concept Unique Identifier: C0342783. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does E71.312 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like short 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 E71.312?
There is no direct ICD-11 mapping available for E71.312 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.