E71.314
BillableMuscle carnitine palmitoyltransferase deficiency
Muscle carnitine palmitoyltransferase deficiency
Coding Notes
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(35)
SNOMED CT
- Amino acid deficiency82994006
- Muscle carnitine deficiency84264005
- Carnitine palmitoyltransferase deficiency90500005
- CPT1 - Carnitine palmitoyltransferase I deficiency238001003
- CPTI - Carnitine palmitoyltransferase deficiency type I238001003
- Carnitine palmitoyltransferase I deficiency238001003
- Carnitine palmitoyltransferase deficiency type 1238001003
- Liver form of carnitine palmitoyltransferase deficiency238001003
- 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
- Carnitine deficiency421784001
- CPT2-gene related myopathic form of carnitine palmitoyltransferase II deficiency1187514002
- Carnitine palmitoyl transferase II deficiency, myopathic form1187514002
- Myopathic form of carnitine palmitoyltransferase II deficiency1187514002
Clinical Terms
- Carnitine palmitoyltransferase I deficiency
- Muscle carnitine deficiency
- Amino acid deficiency
- CPT2-gene related myopathic form of carnitine palmitoyltransferase II deficiency
- CPTII - Carnitine palmitoyltransferase deficiency type II
- CPTI - Carnitine palmitoyltransferase deficiency type I
- Carnitine palmitoyltransferase deficiency
- CPT2 - Carnitine palmitoyltransferase II deficiency
- Carnitine palmitoyltransferase deficiency type 2
- Muscle form of carnitine palmitoyltransferase deficiency
- Carnitine palmitoyl transferase II deficiency, myopathic form
- Carnitine deficiency
- Carnitine palmitoyltransferase II deficiency
- CPT1 - Carnitine palmitoyltransferase I deficiency
- Carnitine palmitoyltransferase deficiency type 1
- Myopathic form of carnitine palmitoyltransferase II deficiency
- Liver form of carnitine palmitoyltransferase deficiency
Frequently Asked Questions
What is the ICD-10 code for muscle carnitine palmitoyltransferase deficiency?
The ICD-10-CM code for muscle carnitine palmitoyltransferase deficiency is E71.314. The full clinical description is "Muscle carnitine palmitoyltransferase deficiency". E71.314 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E71.314 mean?
ICD-10-CM code E71.314 represents “Muscle carnitine palmitoyltransferase 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 E71.314 a billable code?
Yes, E71.314 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E71.314 in?
E71.314 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E71.314?
E71.314 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 E71.314 map to?
E71.314 maps to 7 SNOMED CT concepts: 82994006, 238001003, 238002005, 1187514002, 421784001, and 2 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E71.314?
E71.314 is linked to 1 UMLS Concept Unique Identifier: C2874243. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does E71.314 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like muscle carnitine palmitoyltransferase 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 E71.314?
There is no direct ICD-11 mapping available for E71.314 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.