E71.51Header (non-billable)

Disorders of peroxisome biogenesis

Category
E71
Parent code
E71.5

Code family — category E71

Every other code sharing category E71, for context when choosing between close variants.

E71Header

Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism

Ch. IV
E71.0Billable

Maple-syrup-urine disease

Ch. IV
E71.1Header

Other disorders of branched-chain amino-acid metabolism

Ch. IV
E71.11Header

Branched-chain organic acidurias

Ch. IV
E71.110Billable

Isovaleric acidemia

Ch. IV
E71.111Billable

3-methylglutaconic aciduria

Ch. IV
E71.118Billable

Other branched-chain organic acidurias

Ch. IV
E71.12Header

Disorders of propionate metabolism

Ch. IV
E71.120Billable

Methylmalonic acidemia

Ch. IV
E71.121Billable

Propionic acidemia

Ch. IV
E71.128Billable

Other disorders of propionate metabolism

Ch. IV
E71.19Billable

Other disorders of branched-chain amino-acid metabolism

Ch. IV
E71.2Billable

Disorder of branched-chain amino-acid metabolism, unspecified

Ch. IV
E71.3Header

Disorders of fatty-acid metabolism

Ch. IV
E71.30Billable

Disorder of fatty-acid metabolism, unspecified

Ch. IV
E71.31Header

Disorders of fatty-acid oxidation

Ch. IV
E71.310Billable

Long chain/very long chain acyl CoA dehydrogenase deficiency

Ch. IV
E71.311Billable

Medium chain acyl CoA dehydrogenase deficiency

Ch. IV
E71.312Billable

Short chain acyl CoA dehydrogenase deficiency

Ch. IV
E71.313Billable

Glutaric aciduria type II

Ch. IV
E71.314Billable

Muscle carnitine palmitoyltransferase deficiency

Ch. IV
E71.318Billable

Other disorders of fatty-acid oxidation

Ch. IV
E71.32Billable

Disorders of ketone metabolism

Ch. IV
E71.39Billable

Other disorders of fatty-acid metabolism

Ch. IV
E71.4Header

Disorders of carnitine metabolism

Ch. IV
E71.40Billable

Disorder of carnitine metabolism, unspecified

Ch. IV
E71.41Billable

Primary carnitine deficiency

Ch. IV
E71.42Billable

Carnitine deficiency due to inborn errors of metabolism

Ch. IV
E71.43Billable

Iatrogenic carnitine deficiency

Ch. IV
E71.44Header

Other secondary carnitine deficiency

Ch. IV
E71.440Billable

Ruvalcaba-Myhre-Smith syndrome

Ch. IV
E71.448Billable

Other secondary carnitine deficiency

Ch. IV
E71.5Header

Peroxisomal disorders

Ch. IV
E71.50Billable

Peroxisomal disorder, unspecified

Ch. IV
E71.510Billable

Zellweger syndrome

Ch. IV
E71.511Billable

Neonatal adrenoleukodystrophy

Ch. IV
E71.518Billable

Other disorders of peroxisome biogenesis

Ch. IV
E71.52Header

X-linked adrenoleukodystrophy

Ch. IV
E71.520Billable

Childhood cerebral X-linked adrenoleukodystrophy

Ch. IV
E71.521Billable

Adolescent X-linked adrenoleukodystrophy

Ch. IV
E71.522Billable

Adrenomyeloneuropathy

Ch. IV
E71.528Billable

Other X-linked adrenoleukodystrophy

Ch. IV
E71.529Billable

X-linked adrenoleukodystrophy, unspecified type

Ch. IV
E71.53Billable

Other group 2 peroxisomal disorders

Ch. IV
E71.54Header

Other peroxisomal disorders

Ch. IV
E71.540Billable

Rhizomelic chondrodysplasia punctata

Ch. IV
E71.541Billable

Zellweger-like syndrome

Ch. IV
E71.542Billable

Other group 3 peroxisomal disorders

Ch. IV
E71.548Billable

Other peroxisomal disorders

Ch. IV

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