E71.1 Other disorders of branched-chain amino-acid metabolism

Non-billable header with 3 child codes.

Codes under E71.1

• E71.11 Branched-chain organic acidurias
• E71.12 Disorders of propionate metabolism
• E71.19 Other disorders of branched-chain amino-acid metabolism

Code annotations containing back-references to E71.1

Back-references to E71.1

• Type 1 Excludes: E72 Other disorders of amino-acid metabolism ("branched-chain amino-acid metabolism (E71.0-E71.2)")

Back-references to E71

• Type 2 Excludes: G11 Hereditary ataxia ("metabolic disorders (E70-E88)")
• Code First: G63 Polyneuropathy in diseases classified elsewhere ("metabolic diseases (E70-E88)")
• Type 2 Excludes: G71 Primary disorders of muscles ("metabolic disorders (E70-E88)")
• Code First: H42 Glaucoma in diseases classified elsewhere ("specified metabolic disorder (E70-E88)")
• Type 2 Excludes: N25.0 Renal osteodystrophy ("metabolic disorders classifiable to E70-E88")
• Type 2 Excludes: N25.81 Secondary hyperparathyroidism of renal origin ("metabolic disorders classifiable to E70-E88")
• Type 1 Excludes: P59 Neonatal jaundice from other and unspecified causes ("jaundice due to inborn errors of metabolism (E70-E88)")
• Type 1 Excludes: R79 Other abnormal findings of blood chemistry ("specific findings indicating disorder of amino-acid metabolism (E70-E72)")
• Type 1 Excludes: R79.83 Abnormal findings of blood amino-acid level ("disorders of amino-acid metabolism (E70-E72)")

Nearby codes

• E71 Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism
• E71.0 Maple-syrup-urine disease
• E71.1 Other disorders of branched-chain amino-acid metabolism (this code)
• E71.11 Branched-chain organic acidurias
• E71.110 Isovaleric acidemia
• E71.111 3-methylglutaconic aciduria
• E71.118 Other branched-chain organic acidurias
• E71.12 Disorders of propionate metabolism