5C50
category
Inborn errors of amino acid or other organic acid metabolism
19 subordinate codes
5C50.0Phenylketonuria5C50.1Disorders of tyrosine metabolism5C50.2Disorders of histidine metabolism5C50.3Disorders of tryptophan metabolism5C50.4Disorders of lysine or hydroxylysine metabolism5C50.5Disorders of the gamma-glutamyl cycle5C50.6Disorders of serine metabolism5C50.7Disorders of glycine metabolism5C50.8Disorders of proline or hydroxyproline metabolism5C50.9Disorders of ornithine metabolism5C50.ADisorders of urea cycle metabolism5C50.BDisorders of methionine cycle or sulphur amino acid metabolism5C50.CDisorders of beta or omega amino acid metabolism5C50.DDisorders of branched-chain amino acid metabolism5C50.EOrganic aciduria5C50.FDisorders of peptide metabolism5C50.GTrimethylaminuria4B4YOther specified diseases of the immune system4B4ZDiseases of the immune system, unspecified
Nearby in Inborn errors of metabolism
5C51Inborn errors of carbohydrate metabolism5C52Inborn errors of lipid metabolism5C53Inborn errors of energy metabolism5C54Inborn errors of glycosylation or other specified protein modification5C55Inborn errors of purine, pyrimidine or nucleotide metabolism5C56Lysosomal diseases5C57Peroxisomal diseases5C58Inborn errors of porphyrin or heme metabolism