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 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)
Also Known As / Clinical Terms
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
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.
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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.