E79 Disorders of purine and pyrimidine metabolismNon-billable header with 5 child codes.
E79.0 Hyperuricemia without signs of inflammatory arthritis and tophaceous diseaseE79.1 Lesch-Nyhan syndromeE79.2 Myoadenylate deaminase deficiencyE79.8 Other disorders of purine and pyrimidine metabolismE79.9 Disorder of purine and pyrimidine metabolism, unspecifiedE72 Other disorders of amino-acid metabolism ("purine and pyrimidine metabolism (E79.-)")G11 Hereditary ataxia ("metabolic disorders (E70-E88)")G11.3 Cerebellar ataxia with defective DNA repair ("other disorders of purine and pyrimidine metabolism (E79.-)")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)")E72 Other disorders of amino-acid metabolism ("purine and pyrimidine metabolism (E79.-)")G11 Hereditary ataxia ("metabolic disorders (E70-E88)")G11.3 Cerebellar ataxia with defective DNA repair ("other disorders of purine and pyrimidine metabolism (E79.-)")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)")