Other disorders of amino-acid metabolism
Notes: Fanconi (-de Toni) (-Debré) syndrome with cystinosis ; Fanconi (-de Toni) (-Debré) syndrome, unspecified ; Cystathionine synthase deficiency ; Cystathioninuria ; Methioninemia ; Sulfite oxidase deficiency ; Hyperammonemia ; Glutaric aciduria NOS ; Glutaric aciduria (type I) ; Hydroxylysinemia ; Hyperlysinemia ; Hyperammonemia-Hyperornithinemia-Homocitrullinemia syndrome ; Ornithinemia (types I, II) ; Ornithine transcarbamylase deficiency ; Oxalosis ; Oxaluria ; D-glycericacidemia ; Hyperhydroxyprolinemia ; Hyperprolinemia (types I, II) ; Sarcosinemia ; 4-hydroxybutyric aciduria ; Disorders of GABA metabolism ; GABA metabolic defect ; GABA transaminase deficiency ; GABA-T deficiency ; Gamma-hydroxybutyric aciduria ; SSADHD ; Succinic semialdehyde dehydrogenase deficiency ; Disorders of beta-amino-acid metabolism ; Disorders of gamma-glutamyl cycle ; code for associated glaucoma (H42) ; disorders of: ; aromatic amino-acid metabolism (E70.-) ; branched-chain amino-acid metabolism (E71.0-E71.2) ; fatty-acid metabolism (E71.3) ; purine and pyrimidine metabolism (E79.-) ; gout (M1A.-, M10.-) ; disorders of tryptophan metabolism (E70.5) ; Fanconi (-de Toni) (-Debré) syndrome without cystinosis (E72.09) ; cystinosis (E72.04) ; cystinuria (E72.01) ; transcobalamin II deficiency (D51.2) ; disorders of ornithine metabolism (E72.4) ; hyperammonemia-hyperornithinemia-homocitrullinemia syndrome E72.4 ; transient hyperammonemia of newborn (P74.6) ; glutaric aciduria type II (E71.313) ; Refsum’s disease (G60.1) ; Zellweger syndrome (E71.510) ; hereditary choroidal dystrophy (H31.2-)