5C50.4
category
Disorders of lysine or hydroxylysine metabolism
Exclusions
- Glutaryl-CoA dehydrogenase deficiency
(5C50.E1) - Refsum disease
(5C57.1) - Zellweger syndrome
(5C57.0)
Also indexed as
2-aminoadipic acidaemia2-aminoadipic aciduria2-ketoadipic acidaemia2-ketoadipic aciduria2-oxoadipic acidaemia2-oxoadipic aciduriaAlpha-aminoadipic semialdehyde deficiencyDisorders of lysine or hydroxylysine metabolismHydroxylysine metabolic disorderHydroxylysinemiaHyperlysinaemiaHyperlysinaemia type 1Hyperlysinaemia type 2Lysine alpha-ketoglutarate reductase deficiencyLysine hyperaminoaciduriaLysine intoleranceLysine metabolic disorderPipecolic acidaemiaSaccharopine dehydrogenase deficiencySaccharopinuriaSeizures - intellectual deficit due to hydroxylysinuriaglutaric aciduria NOSoxoglutarate reductase deficiency
Nearby in Inborn errors of amino acid or other organic acid metabolism
5C50.0Phenylketonuria5C50.1Disorders of tyrosine metabolism5C50.2Disorders of histidine metabolism5C50.3Disorders of tryptophan metabolism5C50.5Disorders of the gamma-glutamyl cycle5C50.6Disorders of serine metabolism5C50.7Disorders of glycine metabolism5C50.8Disorders of proline or hydroxyproline metabolism