Skyscape Web Viewer : International Classification of Diseases : ICD10 Index

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[E71.121]-Propionic acidemia
[E71.128] - Other disorders of propionate metabolism
[E71.19]-Hyperleucine-isoleucinemia
[E71.19]-Hypervalinemia
[E71.19]-Isoleucinosis
[E71.19] - Other disorders of branched-chain amino-acid metabolism
[E71.2]-Branched-chain amino-acid disorder
[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]-Carnitine insufficiency
[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
[E71.440]-Ruvalcaba-Myhre-Smith syndrome
[E71.448] - Other secondary carnitine deficiency
[E71.5] - Peroxisomal disorders