E71.318
BillableOther disorders of fatty-acid oxidation
Other disorders of fatty-acid oxidation
Coding Notes
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
- Carnitine palmitoyltransferase deficiency90500005
- Deficiency of 3-hydroxyacyl-CoA dehydrogenase124122005
- Deficiency of beta-hydroxyacyl dehydrogenase124122005
- Deficiency of beta-keto-reductase124122005
- Beta ketothiolase deficiency124265004
- Deficiency of 3-ketoacyl-CoA thiolase124265004
- Deficiency of acetyl-CoA acyltransferase124265004
- Deficiency of acetyl-coenzyme A acyltransferase124265004
- Deficiency of beta-ketothiolase124265004
- Deficiency of enoyl hydrase124621004
- Deficiency of enoyl-CoA hydratase124621004
- Deficiency of enoyl-coenzyme A hydratase124621004
- Deficiency of unsaturated acyl-CoA hydratase124621004
- Enoyl-CoA hydratase deficiency124621004
- Human trifunctional protein deficiency237999008
- Mitochondrial trifunctional protein deficiency237999008
- Trifunctional enzyme deficiency237999008
- Trifunctional protein deficiency237999008
- 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
- CPT2 - Carnitine palmitoyltransferase II deficiency238002005
- CPTII - Carnitine palmitoyltransferase deficiency type II238002005
- Carnitine palmitoyltransferase II deficiency238002005
- Carnitine palmitoyltransferase deficiency type 2238002005
- Muscle form of carnitine palmitoyltransferase deficiency238002005
- 3-Ketoacid CoA transferase deficiency238004006
- Succinyl-CoA 3-ketoacid transferase deficiency238004006
- Succinyl-CoA acetoacetate transferase deficiency238004006
- Succinyl-coenzyme A acetoacetate transferase deficiency238004006
- Thioacyl transferase deficiency238004006
- Isolated long chain hydroxyacyl-CoA dehydrogenase deficiency307127004
- LCHAD - Isolated long chain hydroxyacyl-CoA dehydrogenase deficiency307127004
- Combined long chain hydroxyacyl-CoA dehydrogenase deficiency307128009
- Combined long chain hydroxyacyl-coenzyme A dehydrogenase deficiency307128009
- 3-Ketoacyl-CoA triolase deficiency307130006
- 3-Ketoacyl-coenzyme A triolase deficiency307130006
- Deficiency of 2-methylbutyryl-CoA dehydrogenase444838008
- Deficiency of 2-methylbutyryl-coenzyme A dehydrogenase444838008
- ACAD9 (acyl-CoA dehydrogenase 9) deficiency725046003
- Acyl-CoA dehydrogenase 9 deficiency725046003
- Deficiency of acyl-coenzyme A dehydrogenase 9725046003
- Mitochondrial complex I deficiency due to deficiency of acyl-coenzyme A dehydrogenase 9725046003
- FAOD - fatty acid oxidation defect1156591005
- Fatty acid oxidation defect1156591005
- Fatty acid oxidation disorder1156591005
- Neonatal form of carnitine palmitoyltransferase II deficiency1187511005
- Severe infantile form of carnitine palmitoyltransferase II deficiency1187536004
- Deficiency of isolated LCKAT (long-chain 3-keto-acyl coenzyme A thiolase)1295528005
- Isolated deficiency of long-chain 3-keto-acyl coenzyme A thiolase1295528005
- Isolated long-chain 3-keto-acyl CoA thiolase deficiency1295528005
Frequently Asked Questions
What is the ICD-10 code for other disorders of fatty-acid oxidation?
The ICD-10-CM code for other disorders of fatty-acid oxidation is E71.318. The full clinical description is "Other disorders of fatty-acid oxidation". E71.318 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E71.318 mean?
ICD-10-CM code E71.318 represents "Other disorders of fatty-acid oxidation". 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 E71.318 a billable code?
Yes, E71.318 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E71.318 in?
E71.318 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E71.318?
E71.318 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 E71.318 map to?
E71.318 maps to 17 SNOMED CT concepts: 238004006, 307130006, 725046003, 124265004, 238002005, and 12 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E71.318?
E71.318 is linked to 1 UMLS Concept Unique Identifier: C1829846. 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.