E71.40 Disorder of carnitine metabolism, unspecifiedBillable ICD-10-CM code, FY2026.
Defines the logic of DRG(s) 642 in MDC 10.
277.84 Other secondary carnitine deficiency (approximate)G11 Hereditary ataxia ("metabolic disorders (E70-E88)")G63 Polyneuropathy in diseases classified elsewhere ("metabolic diseases (E70-E88)")G71 Primary disorders of muscles ("metabolic disorders (E70-E88)")H42 Glaucoma in diseases classified elsewhere ("specified metabolic disorder (E70-E88)")N25.0 Renal osteodystrophy ("metabolic disorders classifiable to E70-E88")N25.81 Secondary hyperparathyroidism of renal origin ("metabolic disorders classifiable to E70-E88")P59 Neonatal jaundice from other and unspecified causes ("jaundice due to inborn errors of metabolism (E70-E88)")R79 Other abnormal findings of blood chemistry ("specific findings indicating disorder of amino-acid metabolism (E70-E72)")R79.83 Abnormal findings of blood amino-acid level ("disorders of amino-acid metabolism (E70-E72)")E71.314 Muscle carnitine palmitoyltransferase deficiencyE71.318 Other disorders of fatty-acid oxidationE71.32 Disorders of ketone metabolismE71.39 Other disorders of fatty-acid metabolismE71.4 Disorders of carnitine metabolismE71.40 Disorder of carnitine metabolism, unspecified (this code)E71.41 Primary carnitine deficiencyE71.42 Carnitine deficiency due to inborn errors of metabolismE71.43 Iatrogenic carnitine deficiencyE71.44 Other secondary carnitine deficiencyE71.440 Ruvalcaba-Myhre-Smith syndrome