E70.2 Disorders of tyrosine metabolism

Non-billable header with 3 child codes.

Excludes1 (never code together)

• transitory tyrosinemia of newborn (P74.5)

Codes under E70.2

• E70.20 Disorder of tyrosine metabolism, unspecified
• E70.21 Tyrosinemia
• E70.29 Other disorders of tyrosine metabolism

Code annotations containing back-references to E70.2

Back-references to E70

• Type 1 Excludes: E72 Other disorders of amino-acid metabolism ("aromatic amino-acid metabolism (E70.-)")
• 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

• E70 Disorders of aromatic amino-acid metabolism
• E70.0 Classical phenylketonuria
• E70.1 Other hyperphenylalaninemias
• E70.2 Disorders of tyrosine metabolism (this code)
• E70.20 Disorder of tyrosine metabolism, unspecified
• E70.21 Tyrosinemia
• E70.29 Other disorders of tyrosine metabolism
• E70.3 Albinism
• E70.30 Albinism, unspecified