5C50ICD-11 MMS 2026-01
Inborn errors of amino acid or other organic acid metabolism
Exclusions from above levels
- http://id.who.int/icd/entity/1191191920 – Disorders of lipoprotein metabolism or certain specified lipidaemias
3A10.Z– Hereditary haemolytic anaemia due to enzyme deficiency5A71.01– Congenital adrenal hyperplasia
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Child codes
5C50.0– Phenylketonuria5C50.1– Disorders of tyrosine metabolism5C50.2– Disorders of histidine metabolism5C50.3– Disorders of tryptophan metabolism5C50.4– Disorders of lysine or hydroxylysine metabolism5C50.5– Disorders of the gamma-glutamyl cycle5C50.6– Disorders of serine metabolism5C50.7– Disorders of glycine metabolism5C50.8– Disorders of proline or hydroxyproline metabolism5C50.9– Disorders of ornithine metabolism5C50.A– Disorders of urea cycle metabolism5C50.B– Disorders of methionine cycle or sulphur amino acid metabolism5C50.C– Disorders of beta or omega amino acid metabolism5C50.D– Disorders of branched-chain amino acid metabolism5C50.E– Organic aciduria5C50.F– Disorders of peptide metabolism5C50.G– Trimethylaminuria5C50.Y– Other specified inborn errors of amino acid or other organic acid metabolism5C50.Z– Inborn errors of amino acid or other organic acid metabolism, unspecified
Sibling codes
5C51– Inborn errors of carbohydrate metabolism5C52– Inborn errors of lipid metabolism5C53– Inborn errors of energy metabolism5C54– Inborn errors of glycosylation or other specified protein modification5C55– Inborn errors of purine, pyrimidine or nucleotide metabolism5C56– Lysosomal diseases5C57– Peroxisomal diseases5C58– Inborn errors of porphyrin or heme metabolism5C59– Inborn errors of neurotransmitter metabolism5C5A– Alpha-1-antitrypsin deficiency5C5Y– Other specified inborn errors of metabolism5C5Z– Inborn errors of metabolism, unspecified
Foundation entity
Inborn errors of amino acid or other organic acid metabolism – http://id.who.int/icd/entity/1324115669
Part of: 05: Endocrine, nutritional or metabolic diseases