5C50.9 category

Disorders of ornithine metabolism

Also indexed as

Deficiency of citrulline phosphorylaseDisorders of ornithine metabolismGeneralised gyrate choroid atrophyHOGA - [hyperornithinaemia - gyrate atrophy of choroid and retina]HyperornithinaemiaOAT - [ornithine oxo-acid aminotransferase] deficiencyOKT - [ornithine ketoacid transaminase] deficiencyOrnithinaemiaOrnithinaemia Type 1Ornithinaemia Type 2Ornithine aminotransferase deficiencyOrnithine hyperaminoaciduriaOrnithine keto-acid transaminase deficiencyOrnithine oxo-acid aminotransferase deficiencyOrnithine-delta-aminotransferase deficiencyornithine-oxo-acid amino acid transferase deficiency

Nearby in Inborn errors of amino acid or other organic acid metabolism

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