E71.31
Non-billableDisorders of fatty-acid oxidation
Disorders of fatty-acid oxidation
This is a header/category code. For billing purposes, use a more specific child code from the list below.
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)
Child Codes (6)
E71.310Long chain/very long chain acyl CoA dehydrogenase deficiency
E71.311Medium chain acyl CoA dehydrogenase deficiency
E71.312Short chain acyl CoA dehydrogenase deficiency
E71.313Glutaric aciduria type II
E71.314Muscle carnitine palmitoyltransferase deficiency
E71.318Other disorders of fatty-acid oxidation
Also Known As / Clinical Terms
Frequently Asked Questions
What is the ICD-10 code for disorders of fatty-acid oxidation?
The ICD-10-CM code for disorders of fatty-acid oxidation is E71.31. The full clinical description is "Disorders of fatty-acid oxidation". E71.31 is a non-billable header code. Use a more specific child code for billing purposes.
What does ICD-10 code E71.31 mean?
ICD-10-CM code E71.31 represents "Disorders of fatty-acid oxidation". It is classified under Chapter 4: Endocrine, Nutritional and Metabolic Diseases and is a non-billable header code. Use a more specific child code for billing purposes.
Is E71.31 a billable code?
No, E71.31 is a non-billable header code. You need to use one of its more specific child codes for billing. There are 6 child codes under E71.31.
What chapter is E71.31 in?
E71.31 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E71.31?
E71.31 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 are the subcategories under E71.31?
E71.31 has 6 child codes, including: E71.310 (Long chain/very long chain acyl CoA dehydrogenase deficiency), E71.311 (Medium chain acyl CoA dehydrogenase deficiency), E71.312 (Short chain acyl CoA dehydrogenase deficiency), E71.313 (Glutaric aciduria type II), and 2 more.
What are the UMLS CUIs for E71.31?
E71.31 is linked to 1 UMLS Concept Unique Identifier: C1456270. 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.