Code family — category E71
Every other code sharing category E71, for context when choosing between close variants.
Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism
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
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
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