Maple-syrup-urine disease

Other disorders of branched-chain amino-acid metabolism

Branched-chain organic acidurias

Isovaleric acidemia

3-methylglutaconic aciduria

Other branched-chain organic acidurias

Disorders of propionate metabolism

Methylmalonic acidemia

Propionic acidemia

Other disorders of propionate metabolism

Other disorders of branched-chain amino-acid metabolism

Disorder of branched-chain amino-acid metabolism, unspecified

Disorders of fatty-acid metabolism

Disorder of fatty-acid metabolism, unspecified

Disorders of fatty-acid oxidation

Long chain/very long chain acyl CoA dehydrogenase deficiency

Medium chain acyl CoA dehydrogenase deficiency

Short chain acyl CoA dehydrogenase deficiency

Glutaric aciduria type II

Muscle carnitine palmitoyltransferase deficiency

Other disorders of fatty-acid oxidation

Disorders of ketone metabolism

Other disorders of fatty-acid metabolism

Disorders of carnitine metabolism

Disorder of carnitine metabolism, unspecified

Primary carnitine deficiency

Carnitine deficiency due to inborn errors of metabolism

Iatrogenic carnitine deficiency

Other secondary carnitine deficiency

Ruvalcaba-Myhre-Smith syndrome

Other secondary carnitine deficiency

Peroxisomal disorders

Peroxisomal disorder, unspecified

Disorders of peroxisome biogenesis

Zellweger syndrome

Neonatal adrenoleukodystrophy

Other disorders of peroxisome biogenesis

X-linked adrenoleukodystrophy

Childhood cerebral X-linked adrenoleukodystrophy

Adolescent X-linked adrenoleukodystrophy

Adrenomyeloneuropathy

Other X-linked adrenoleukodystrophy

X-linked adrenoleukodystrophy unspecified type

Other group 2 peroxisomal disorders

Other peroxisomal disorders

Rhizomelic chondrodysplasia punctata

Zellweger-like syndrome

Other group 3 peroxisomal disorders

Other peroxisomal disorders