Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism
Notes: Hyperleucine-isoleucinemia ; Hypervalinemia ; LCAD ; VLCAD ; MCAD ; SCAD ; Glutaric aciduria type II A ; Glutaric aciduria type II B ; Glutaric aciduria type II C ; Carnitine deficiency due to hemodialysis ; Carnitine deficiency due to Valproic acid therapy ; Group 1 peroxisomal disorders ; Addison only phenotype adrenoleukodystrophy ; Addison-Schilder adrenoleukodystrophy ; peroxisomal disorders (E71.5) ; Refsum’s disease (G60.1) ; Schilder’s disease (G37.0) ; glutaric aciduria (type 1) NOS (E72.3) ; Muscle carnitine palmitoyltransferase deficiency (E71.314) ; Schilder’s disease (G37.0) ; Refsum’s disease (G60.1) ; X-linked adrenoleukodystrophy (E71.42-) ; chondrodysplasia punctata NOS (Q77.3) ; carnitine deficiency due to inborn error of metabolism (E71.42)