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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