E71.39
BillableOther disorders of fatty-acid metabolism
Other disorders of fatty-acid metabolism
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
- Acetyl-CoA carboxylase deficiency4920001
- Deficiency of acetyl-CoA carboxylase4920001
- Deficiency of acetyl-coenzyme A carboxylase4920001
- Deficiency of acetoacetyl-CoA reductase124123000
- Deficiency of acetoacetyl-coenzyme A reductase124123000
- Deficiency of 2-hydroxyglutarate dehydrogenase124149005
- Deficiency of dehydrogenase124226002
- Deficiency of carnitine acetyltransferase124257002
- Deficiency of coenzyme-A transferase124404001
- Beta-hydroxyisobutyryl-coenzyme A deacylase deficiency124427009
- Deficiency of 3-hydroxyisobutyryl CoA hydrolase124427009
- Deficiency of 3-hydroxyisobutyryl coenzyme A hydrolase124427009
- Deficiency of malonyl-CoA decarboxylase124594007
- Deficiency of malonyl-coenzyme A decarboxylase124594007
- Malonyl-CoA decarboxylase deficiency124594007
- Deficiency of 3-hydroxybutyryl-CoA epimerase124660002
- Deficiency of 3-hydroxybutyryl-coenzyme A epimerase124660002
- Deficiency of 1 biotinyl-CoA synthetase124698002
- Deficiency of acetate thiokinase124698002
- Deficiency of acetate-CoA ligase124698002
- Deficiency of acetate-coenzyme A ligase124698002
- Deficiency of acetyl activating enzyme124698002
- Deficiency of acetyl-CoA synthetase124698002
- Deficiency of acyl-CoA synthetase124699005
- Deficiency of fatty acid thiokinase (long chain)124699005
- Deficiency of long-chain-fatty-acid-CoA ligase124699005
- Deficiency of glutarate-CoA ligase124702003
- Deficiency of glutaryl-CoA synthetase124702003
- Carnitine acylcarnitine translocase deficiency238003000
- Deficiency of acetyl-CoA deacylase360709003
- Deficiency of acetyl-coenzyme A deacylase360709003
- Deficiency of acetyl-CoA acylase360721004
- Deficiency of acetyl-coenzyme A acylase360721004
- Deficiency of acetyl-CoA hydrolase360733009
- Deficiency of long-chain fatty-acyl-CoA hydrolase360757009
- Deficiency of long-chain fatty-acyl-coenzyme A hydrolase360757009
- Deficiency of palmitoyl-CoA hydrolase360757009
- Deficiency of palmitoyl-coenzyme A hydrolase360757009
- MLYCD-gene related malonic aciduria361203007
- Malonic aciduria361203007
- Long-chain fatty acid transport deficiency426387005
- Deficiency of 2,4-dienoyl-CoA reductase444944006
- Deficiency of 2,4-dienoyl-coenzyme A reductase444944006
- 3-hydroxy-3-methylglutaryl-CoA synthase deficiency725286002
- 3-hydroxy-3-methylglutaryl-coenzyme A synthase deficiency725286002
- Deficiency of 3-hydroxy-3-methylglutaryl-coenzyme A synthase725286002
- HMG-coenzyme A synthase deficiency725286002
- LCHADD - long chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency726021008
- Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency726021008
- Long chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency726021008
Frequently Asked Questions
What is the ICD-10 code for other disorders of fatty-acid metabolism?
The ICD-10-CM code for other disorders of fatty-acid metabolism is E71.39. The full clinical description is "Other disorders of fatty-acid metabolism". E71.39 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E71.39 mean?
ICD-10-CM code E71.39 represents "Other disorders of fatty-acid metabolism". 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 E71.39 a billable code?
Yes, E71.39 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E71.39 in?
E71.39 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E71.39?
E71.39 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 E71.39 map to?
E71.39 maps to 22 SNOMED CT concepts: 725286002, 4920001, 124427009, 238003000, 124698002, and 17 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E71.39?
E71.39 is linked to 1 UMLS Concept Unique Identifier: C2874245. 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.