E71.41
BillablePrimary carnitine deficiency
Primary carnitine deficiency
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)
- Muscle carnitine palmitoyltransferase deficiency (E71.314)
Excludes 2
Conditions not included here, but the patient may have both
- Ehlers-Danlos syndromes (Q79.6-)
Also Known As / Clinical Terms
SNOMED CT
UMLS
- CARNITINE DEFICIENCY, PRIMARYC0342788
- CARNITINE DEFICIENCY, SYSTEMIC PRIMARYC0342788
- CARNITINE DEFICIENCY, SYSTEMIC, DUE TO DEFECT IN RENAL REABSORPTION OF CARNITINEC0342788
- CARNITINE TRANSPORTER, PLASMA-MEMBRANE, DEFICIENCY OFC0342788
- CARNITINE UPTAKE DEFECTC0342788
- CDSPC0342788
- CUDC0342788
- Carnitine Transporter DeficiencyC0342788
- Carnitine Uptake DeficiencyC0342788
- Carnitine deficiency, primaryC0342788
- Carnitine deficiency, systemic primaryC0342788
- Carnitine deficiency, systemic, due to defect in renal reabsorption of carnitineC0342788
- Carnitine transporter deficiencyC0342788
- Carnitine transporter, plasma-membrane, deficiency ofC0342788
- Carnitine uptake defectC0342788
- Carnitine uptake deficiencyC0342788
- Primary Carnitine DeficiencyC0342788
- Primary carnitine deficiencyC0342788
- Renal Carnitine Transport DefectC0342788
- Renal carnitine transport defectC0342788
- Renal carnitine transport defect (disorder)C0342788
- SCDC0342788
- SLC22A5-gene related renal carnitine transport defectC0342788
- SYSTEMIC CARNITINE DEFICIENCYC0342788
- Systemic Primary Carnitine DeficiencyC0342788
- Systemic carnitine deficiencyC0342788
- Systemic primary carnitine deficiencyC0342788
- primary carnitine deficiencyC0342788
- systemic carnitine deficiencyC0342788
Frequently Asked Questions
What is the ICD-10 code for primary carnitine deficiency?
The ICD-10-CM code for primary carnitine deficiency is E71.41. The full clinical description is "Primary carnitine deficiency". E71.41 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E71.41 mean?
ICD-10-CM code E71.41 represents "Primary carnitine 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 E71.41 a billable code?
Yes, E71.41 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E71.41 in?
E71.41 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E71.41?
E71.41 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 4 more.
What SNOMED CT codes does E71.41 map to?
E71.41 maps to 1 SNOMED CT concept: 21764004. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E71.41?
E71.41 is linked to 1 UMLS Concept Unique Identifier: C0342788. 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.