Child codes (3)
More specific codes that fall directly under E71.51.
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
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
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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