E71.11 Branched-chain organic aciduriasNon-billable header with 3 child codes.
E71.110 Isovaleric acidemiaE71.111 3-methylglutaconic aciduriaE71.118 Other branched-chain organic aciduriasE72 Other disorders of amino-acid metabolism ("branched-chain amino-acid metabolism (E71.0-E71.2)")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 Disorders of branched-chain amino-acid metabolism and fatty-acid metabolismE71.0 Maple-syrup-urine diseaseE71.1 Other disorders of branched-chain amino-acid metabolismE71.11 Branched-chain organic acidurias (this code)E71.110 Isovaleric acidemiaE71.111 3-methylglutaconic aciduriaE71.118 Other branched-chain organic aciduriasE71.12 Disorders of propionate metabolismE71.120 Methylmalonic acidemia