ICD Data
ABOUT
SERVICES
PORTFOLIO
PRICING
CONTACT
ICD Data
/E00-E89/E70-E88/E71
Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism E71
Codes
• E71.0
Maple-syrup-urine disease
• E71.1
Other disorders of branched-chain amino-acid metabolism
• E71.11
Branched-chain organic acidurias
• E71.110
Isovaleric acidemia
• E71.111
3-methylglutaconic aciduria
• E71.118
Other branched-chain organic acidurias
• E71.12
Disorders of propionate metabolism
• E71.120
Methylmalonic acidemia
• E71.121
Propionic acidemia
• E71.128
Other disorders of propionate metabolism
• E71.19
Other disorders of branched-chain amino-acid metabolism
• E71.2
Disorder of branched-chain amino-acid metabolism, unspecified
• E71.3
Disorders of fatty-acid metabolism
• E71.30
Disorder of fatty-acid metabolism, unspecified
• E71.31
Disorders of fatty-acid oxidation
• E71.310
Long chain/very long chain acyl CoA dehydrogenase deficiency
• E71.311
Medium chain acyl CoA dehydrogenase deficiency
• E71.312
Short chain acyl CoA dehydrogenase deficiency
• E71.313
Glutaric aciduria type II
• E71.314
Muscle carnitine palmitoyltransferase deficiency
• E71.318
Other disorders of fatty-acid oxidation
• E71.32
Disorders of ketone metabolism
• E71.39
Other disorders of fatty-acid metabolism
• E71.4
Disorders of carnitine metabolism
• E71.40
Disorder of carnitine metabolism, unspecified
• E71.41
Primary carnitine deficiency
• E71.42
Carnitine deficiency due to inborn errors of metabolism
• E71.43
Iatrogenic carnitine deficiency
• E71.44
Other secondary carnitine deficiency
• E71.440
Ruvalcaba-Myhre-Smith syndrome
• E71.448
Other secondary carnitine deficiency
• E71.5
Peroxisomal disorders
• E71.50
Peroxisomal disorder, unspecified
• E71.51
Disorders of peroxisome biogenesis
• E71.510
Zellweger syndrome
• E71.511
Neonatal adrenoleukodystrophy
• E71.518
Other disorders of peroxisome biogenesis
• E71.52
X-linked adrenoleukodystrophy
• E71.520
Childhood cerebral X-linked adrenoleukodystrophy
• E71.521
Adolescent X-linked adrenoleukodystrophy
• E71.522
Adrenomyeloneuropathy
• E71.528
Other X-linked adrenoleukodystrophy
• E71.529
…… unspecified type
• E71.53
Other group 2 peroxisomal disorders
• E71.54
Other peroxisomal disorders
• E71.540
Rhizomelic chondrodysplasia punctata
• E71.541
Zellweger-like syndrome
• E71.542
Other group 3 peroxisomal disorders
• E71.548
Other peroxisomal disorders