ICD-10-CM code "E71.41": Primary carnitine deficiency (2024)

Overview

ICD-10 CodeE71.41
DescriptionPrimary carnitine deficiency
Hierarchy
  1. Endocrine, nutritional and metabolic diseases (E00-E89)
  2. Metabolic disorders (E70-E88)
  3. Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism (E71)
  4. Disorders of carnitine metabolism (E71.4)
  5. Primary carnitine deficiency (E71.41)
Billable statusICD-10-CM Billable code

Excludes

  1. Endocrine, nutritional and metabolic diseases (E00-E89)

    Type 1transitory endocrine and metabolic disorders specific to newborn (P70-P74)

  2. Metabolic disorders (E70-E88)

    Type 1androgen insensitivity syndrome (E34.5-)

    Type 1congenital adrenal hyperplasia (E25.0)

    Type 1hemolytic anemias attributable to enzyme disorders (D55.-)

    Type 1Marfan syndrome (Q87.4-)

    Type 15-alpha-reductase deficiency (E29.1)

    Type 2Ehlers-Danlos syndromes (Q79.6-)

  3. Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism (E71)
  4. Disorders of carnitine metabolism (E71.4)

    Type 1Muscle carnitine palmitoyltransferase deficiency (E71.314)

  5. Primary carnitine deficiency (E71.41)

Includes

  1. Endocrine, nutritional and metabolic diseases (E00-E89)
  2. Metabolic disorders (E70-E88)
  3. Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism (E71)
  4. Disorders of carnitine metabolism (E71.4)
  5. Primary carnitine deficiency (E71.41)