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deficit acyl-CoA dehydrogenázy, mnohopočetný

  1. Record numberd054069
    Date06.06.2025
    TypeM
    Topical termdeficit acyl-CoA dehydrogenázy, mnohopočetný
    Other termSlovak (Pseudonym) deficit acylkoenzým A dehydrogenázy, viacnásobný
    Slovak (Pseudonym) acidúria glutárova, typ IIA
    Slovak (Pseudonym) acidúria glutárova, typ IIB
    Slovak (Pseudonym) acidúria glutárova, typ IIC
    Slovak (Pseudonym) acidúria glutárova, typ 2
    Slovak (Pseudonym) acidémia glutárova II
    Slovak (Pseudonym) deficit FAD dehydrogenázy, mnohopočetný
    UDCC16.320.565.100.614C18.452.648.100.614C18.452.660.612
    NoteAn 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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