E71.5 Peroxisomal disordersNon-billable header with 5 child codes.
E71.50 Peroxisomal disorder, unspecifiedE71.51 Disorders of peroxisome biogenesisE71.52 X-linked adrenoleukodystrophyE71.53 Other group 2 peroxisomal disordersE71.54 Other peroxisomal disordersE71.3 Disorders of fatty-acid metabolism ("peroxisomal disorders (E71.5)")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)")E71.42 Carnitine deficiency due to inborn errors of metabolismE71.43 Iatrogenic carnitine deficiencyE71.44 Other secondary carnitine deficiencyE71.440 Ruvalcaba-Myhre-Smith syndromeE71.448 Other secondary carnitine deficiencyE71.5 Peroxisomal disorders (this code)E71.50 Peroxisomal disorder, unspecifiedE71.51 Disorders of peroxisome biogenesisE71.510 Zellweger syndromeE71.511 Neonatal adrenoleukodystrophyE71.518 Other disorders of peroxisome biogenesis