AutoICD API

E71.314

Billable

Muscle carnitine palmitoyltransferase deficiency

Muscle carnitine palmitoyltransferase deficiency

Status

Billable / Specific

Block

E70-E88

Parent Code

E71.31

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)

Excludes 2

Conditions not included here, but the patient may have both

  • Ehlers-Danlos syndromes (Q79.6-)
  • carnitine deficiency due to inborn error of metabolism (E71.42)

Also Known As / Clinical Terms

SNOMED CT

UMLS

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.

Automate ICD-10 Coding With AI

Send clinical text to the AutoICD API and get back structured ICD-10 codes with confidence scores. Integrates into any EHR or billing system in minutes.

Try FreeView API Docs

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.