Other hyperphenylalaninemias
E70.329 Oculocutaneous albinism, unspecified
Oculocutaneous albinism, unspecified
E71 Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism Notes: Hyperleucine-isoleucinemia ; Hyperval…
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 aci ...
E71.310 Long chain/very long chain acyl CoA dehydrogenase deficiency Notes: LCAD ; VLCAD
Long chain/very long chain acyl CoA dehydrogenase deficiency Notes: LCAD ; VLCAD
E71.5 Peroxisomal disorders Notes: Group 1 peroxisomal disorders ; Addison only phenotype adrenoleukodystrophy ; Addison-Schil…
Peroxisomal disorders Notes: Group 1 peroxisomal disorders ; Addison only phenotype adrenoleukodystrophy ; Addison-Schilder adrenoleukodystrophy ; Schilder's disease (G37.0) ; Refsum's disease (G60.1) ...
E71.542 Other group 3 peroxisomal disorders
Other group 3 peroxisomal disorders
E72.20 Disorder of urea cycle metabolism, unspecified Notes: Hyperammonemia ; hyperammonemia-hyperornithinemia-homocitrullinemi…
Disorder of urea cycle metabolism, unspecified Notes: Hyperammonemia ; hyperammonemia-hyperornithinemia-homocitrullinemia syndrome E72.4 ; transient hyperammonemia of newborn (P74.6)
E72.9 Disorder of amino-acid metabolism, unspecified
Disorder of amino-acid metabolism, unspecified