5C50 Inborn errors of amino acid or other organic acid metabolism

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

sections/codes in this section (5C50-5C50)

• Phenylketonuria  (5C50.0)
• Disorders of tyrosine metabolism  (5C50.1)
• Disorders of histidine metabolism  (5C50.2)
• Disorders of tryptophan metabolism  (5C50.3)
• Disorders of lysine or hydroxylysine metabolism  (5C50.4)
• Disorders of the gamma-glutamyl cycle  (5C50.5)
• Disorders of serine metabolism  (5C50.6)
• Disorders of glycine metabolism  (5C50.7)
• Disorders of proline or hydroxyproline metabolism  (5C50.8)
• Disorders of ornithine metabolism  (5C50.9)
• Disorders of urea cycle metabolism  (5C50.A)
• Disorders of methionine cycle or sulphur amino acid metabolism  (5C50.B)
• Disorders of beta or omega amino acid metabolism  (5C50.C)
• Disorders of branched-chain amino acid metabolism  (5C50.D)
• Organic aciduria  (5C50.E)
• Disorders of peptide metabolism  (5C50.F)
• Trimethylaminuria  (5C50.G)
• Other specified inborn errors of amino acid or other organic acid metabolism  (5C50.Y)
• Inborn errors of amino acid or other organic acid metabolism, unspecified  (5C50.Z)

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