ICD 10 Diagnosis Codes related to Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism (50 entries)
Chapter: Endocrine, nutritional and metabolic diseases (E00-E89)| Click on a code to view full code details |
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E71 - Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism
E710 - Maple-syrup-urine disease
E711 - Other disorders of branched-chain amino-acid metabolism
E711.1 - Branched-chain organic acidurias
E711.10 - Isovaleric acidemia
E711.11 - 3-methylglutaconic aciduria
E711.18 - Other branched-chain organic acidurias
E711.2 - Disorders of propionate metabolism
E711.20 - Methylmalonic acidemia
E711.21 - Propionic acidemia
E711.28 - Other disorders of propionate metabolism
E711.9 - Other disorders of branched-chain amino-acid metabolism
E712 - Disorder of branched-chain amino-acid metabolism, unspecified
E713 - Disorders of fatty-acid metabolism
E713.0 - Disorder of fatty-acid metabolism, unspecified
E713.1 - Disorders of fatty-acid oxidation
E713.10 - Long chain/very long chain acyl CoA dehydrogenase deficiency
E713.11 - Medium chain acyl CoA dehydrogenase deficiency
E713.12 - Short chain acyl CoA dehydrogenase deficiency
E713.13 - Glutaric aciduria type II
E713.14 - Muscle carnitine palmitoyltransferase deficiency
E713.18 - Other disorders of fatty-acid oxidation
E713.2 - Disorders of ketone metabolism
E713.9 - Other disorders of fatty-acid metabolism
E714 - Disorders of carnitine metabolism
E714.0 - Disorder of carnitine metabolism, unspecified
E714.1 - Primary carnitine deficiency
E714.2 - Carnitine deficiency due to inborn errors of metabolism
E714.3 - Iatrogenic carnitine deficiency
E714.4 - Other secondary carnitine deficiency
E714.40 - Ruvalcaba-Myhre-Smith syndrome
E714.48 - Other secondary carnitine deficiency
E715 - Peroxisomal disorders
E715.0 - Peroxisomal disorder, unspecified
E715.1 - Disorders of peroxisome biogenesis
E715.10 - Zellweger syndrome
E715.11 - Neonatal adrenoleukodystrophy
E715.18 - Other disorders of peroxisome biogenesis
E715.2 - X-linked adrenoleukodystrophy
E715.20 - Childhood cerebral X-linked adrenoleukodystrophy
E715.21 - Adolescent X-linked adrenoleukodystrophy
E715.22 - Adrenomyeloneuropathy
E715.28 - Other X-linked adrenoleukodystrophy
E715.29 - X-linked adrenoleukodystrophy, unspecified type
E715.3 - Other group 2 peroxisomal disorders
E715.4 - Other peroxisomal disorders
E715.40 - Rhizomelic chondrodysplasia punctata
E715.41 - Zellweger-like syndrome
E715.42 - Other group 3 peroxisomal disorders
E715.48 - Other peroxisomal disorders
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