5C50Level 4

Inborn errors of amino acid or other organic acid metabolism

GET/api/v1/systems/icd_11/nodes/5C50

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5C50.0Phenylketonuria

5C50.1Disorders of tyrosine metabolism

5C50.2Disorders of histidine metabolism

5C50.3Disorders of tryptophan metabolism

5C50.4Disorders of lysine or hydroxylysine metabolism

5C50.5Disorders of the gamma-glutamyl cycle

5C50.6Disorders of serine metabolism

5C50.7Disorders of glycine metabolism

5C50.8Disorders of proline or hydroxyproline metabolism

5C50.9Disorders of ornithine metabolism

5C50.ADisorders of urea cycle metabolism

5C50.BDisorders of methionine cycle or sulphur amino acid metabolism

5C50.CDisorders of beta or omega amino acid metabolism

5C50.DDisorders of branched-chain amino acid metabolism

5C50.EOrganic aciduria

5C50.FDisorders of peptide metabolism

5C50.GTrimethylaminuria

5C50.YOther specified inborn errors of amino acid or other organic acid metabolism

5C50.ZInborn errors of amino acid or other organic acid metabolism, unspecified

Cross-system equivalences0

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