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deficit acyl-CoA dehydrogenázy, mnohopočetný

  1. Subject h.deficit acyl-CoA dehydrogenázy, mnohopočetný
    Subject h.Multiple Acyl Coenzyme A Dehydrogenase Deficiency
    Entry termsdeficit acylkoenzým A dehydrogenázy, viacnásobný
    acidúria glutárova, typ IIA
    acidúria glutárova, typ IIB
    acidúria glutárova, typ IIC
    acidúria glutárova, typ 2
    acidémia glutárova II
    deficit FAD dehydrogenázy, mnohopočetný
    Scope note in EnglishAn autosomal recessive disorder of fatty acid oxidation, and branched chain amino acids (AMINO ACIDS, BRANCHED-CHAIN); LYSINE; and CHOLINE catabolism, that is due to defects in either subunit of ELECTRON TRANSFER FLAVOPROTEIN or its dehydrogenase, electron transfer flavoprotein-ubiquinone oxidoreductase (EC 1.5.5.1).
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