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Taxonomy Codes
Endocrine, nutritional and metabolic diseases
Metabolic disorders (E70-E88)
Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism (E71)
E71
- Disord of branched-chain amino-acid metab & fatty-acid metab
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, unsp
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
- X-linked adrenoleukodystrophy, 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