5C50.9 Disorders of ornithine metabolism

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

code elsewhere

• Hyperornithinaemia-hyperammonaemia-homocitrullinuria  (5C50.AY)
• Ornithine carbamoyltransferase deficiency  (5C50.AY)

synonyms

• Disorders of ornithine metabolism
• Hyperornithinaemia
• Ornithinaemia
• Ornithine aminotransferase deficiency
• Generalised gyrate choroid atrophy
• Ornithine oxo-acid aminotransferase deficiency
• HOGA - [hyperornithinaemia - gyrate atrophy of choroid and retina]
• ornithine-oxo-acid amino acid transferase deficiency
• OKT - [ornithine ketoacid transaminase] deficiency
• OAT - [ornithine oxo-acid aminotransferase] deficiency
• Ornithine keto-acid transaminase deficiency
• Ornithinaemia Type 1
• Ornithinaemia Type 2
• Deficiency of citrulline phosphorylase
• Ornithine hyperaminoaciduria
• Ornithine-delta-aminotransferase deficiency

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