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The ICD-10 code for Carnitine deficiency due to inborn errors of metabolism is E71.42.2026 ICD-10-CM Diagnosis Code E71.42 – Carnitine deficiency due to inborn errors of metabolism Related ICD-10 Codes Parent code: E71 – Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism Other codes in same category: E71.0 – Maple-syrup-urine disease, E71.1 – Other disorders…

The ICD-10 code for Primary carnitine deficiency is E71.41.2026 ICD-10-CM Diagnosis Code E71.41 – Primary carnitine deficiency Related ICD-10 Codes Parent code: E71 – Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism Other codes in same category: E71.0 – Maple-syrup-urine disease, E71.1 – Other disorders of branched-chain amino-acid metabolism, E71.11 – Branched-chain organic acidurias, E71.110…

The ICD-10 code for Disorder of carnitine metabolism, unspecified is E71.40.2026 ICD-10-CM Diagnosis Code E71.40 – Disorder of carnitine metabolism, unspecified Related ICD-10 Codes Parent code: E71 – Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism Other codes in same category: E71.0 – Maple-syrup-urine disease, E71.1 – Other disorders of branched-chain amino-acid metabolism, E71.11 –…

The ICD-10 code for Disorders of carnitine metabolism is E71.4.2026 ICD-10-CM Diagnosis Code E71.4 – Disorders of carnitine metabolism Related ICD-10 Codes Parent code: E71 – Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism Other codes in same category: E71.0 – Maple-syrup-urine disease, E71.1 – Other disorders of branched-chain amino-acid metabolism, E71.11 – Branched-chain organic…

The ICD-10 code for Other disorders of fatty-acid metabolism is E71.39.2026 ICD-10-CM Diagnosis Code E71.39 – Other disorders of fatty-acid metabolism Related ICD-10 Codes Parent code: E71 – Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism Other codes in same category: E71.0 – Maple-syrup-urine disease, E71.1 – Other disorders of branched-chain amino-acid metabolism, E71.11 –…

The ICD-10 code for Disorders of ketone metabolism is E71.32.2026 ICD-10-CM Diagnosis Code E71.32 – Disorders of ketone metabolism Related ICD-10 Codes Parent code: E71 – Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism Other codes in same category: E71.0 – Maple-syrup-urine disease, E71.1 – Other disorders of branched-chain amino-acid metabolism, E71.11 – Branched-chain organic…

The ICD-10 code for Other disorders of fatty-acid oxidation is E71.318.2026 ICD-10-CM Diagnosis Code E71.318 – Other disorders of fatty-acid oxidation Related ICD-10 Codes Parent code: E71 – Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism Other codes in same category: E71.0 – Maple-syrup-urine disease, E71.1 – Other disorders of branched-chain amino-acid metabolism, E71.11 –…

The ICD-10 code for Muscle carnitine palmitoyltransferase deficiency is E71.314.2026 ICD-10-CM Diagnosis Code E71.314 – Muscle carnitine palmitoyltransferase deficiency Related ICD-10 Codes Parent code: E71 – Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism Other codes in same category: E71.0 – Maple-syrup-urine disease, E71.1 – Other disorders of branched-chain amino-acid metabolism, E71.11 – Branched-chain organic…

The ICD-10 code for Glutaric aciduria type II is E71.313. 2026 ICD-10-CM Diagnosis Code E71.313 – Glutaric aciduria type II Related ICD-10 Codes Parent code: E71 – Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism Other codes in same category: E71.0 – Maple-syrup-urine disease, E71.1 – Other disorders of branched-chain amino-acid metabolism, E71.11 – Branched-chain…

The ICD-10 code for Short chain acyl CoA dehydrogenase deficiency is E71.312.2026 ICD-10-CM Diagnosis Code E71.312 – Short chain acyl CoA dehydrogenase deficiency Related ICD-10 Codes Parent code: E71 – Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism Other codes in same category: E71.0 – Maple-syrup-urine disease, E71.1 – Other disorders of branched-chain amino-acid metabolism,…