ICD-11 classes
05 Endocrine, nutritional or metabolic diseases
Metabolic disorders
Inborn errors of metabolism
5C50 — Inborn errors of amino acid or other organic acid metabolism
ICD-11 5C50 — Inborn errors of amino acid or other organic acid metabolism
The diagnosis has no description.
The diagnosis includes nothing.
The diagnosis excludes nothing.
Diagnosis with code 5C50 contains 19 clarifying diagnoses:
- 5C50.0 — Phenylketonuria
It contains 5 clarifying diagnoses. - 5C50.1 — Disorders of tyrosine metabolism
It contains 6 clarifying diagnoses. - 5C50.2 — Disorders of histidine metabolism
It contains 4 clarifying diagnoses. - 5C50.3 — Disorders of tryptophan metabolism
- 5C50.4 — Disorders of lysine or hydroxylysine metabolism
- 5C50.5 — Disorders of the gamma-glutamyl cycle
- 5C50.6 — Disorders of serine metabolism
- 5C50.7 — Disorders of glycine metabolism
It contains 4 clarifying diagnoses. - 5C50.8 — Disorders of proline or hydroxyproline metabolism
- 5C50.9 — Disorders of ornithine metabolism
- 5C50.A — Disorders of urea cycle metabolism
It contains 6 clarifying diagnoses. - 5C50.B — Disorders of methionine cycle or sulphur amino acid metabolism
- 5C50.C — Disorders of beta or omega amino acid metabolism
- 5C50.D — Disorders of branched-chain amino acid metabolism
It contains 3 clarifying diagnoses. - 5C50.E — Organic aciduria
It contains 4 clarifying diagnoses. - 5C50.F — Disorders of peptide metabolism
It contains 5 clarifying diagnoses. - 5C50.G — Trimethylaminuria
- 5C50.Y — Other specified inborn errors of amino acid or other organic acid metabolism
- 5C50.Z — Inborn errors of amino acid or other organic acid metabolism, unspecified