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Hyperlysinemia

Overview

Related in the Kosmos

Inborn errors of metabolism
- 3 methylcrotonyl-coa carboxylase deficiency
- 2-Methylbutyryl-CoA dehydrogenase deficiency

Genetic disorder

Autosomal recessive disorders
- Saccharopinuria
- 3 methylcrotonyl-coa carboxylase deficiency

Genetic disorders

Medical condition
- Saccharopinuria
- 6-pyruvoyl- tetrahydropterin synthase deficiency

Diseases and disorders
- Saccharopinuria

See also