Number of the records: 1
deficit acyl-CoA dehydrogenázy, mnohopočetný
SYS d054069 LBL 00000cx--j2200000---45-- 005 20240119200555.8 100 $a 20080101asloy0103----ba0 152 $b mesh 250 $a deficit acyl-CoA dehydrogenázy, mnohopočetný $x BL $x CF $x CI $x CL $x CO $x DG $x DH $x DI $x DT $x EC $x EH $x EM $x EN $x EP $x ET $x GE $x HI $x IM $x ME $x MI $x MO $x NU $x PA $x PC $x PP $x PS $x PX $x RH $x RT $x SU $x TH $x UR $x VE $x VI $8 slo 300 1-
$a 2008 $8 eng 330 1-
$a An 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). $8 eng 450 $a deficit acylkoenzým A dehydrogenázy, viacnásobný $5 e $8 slo 450 $a acidúria glutárova, typ IIA $5 e $8 slo 450 $a acidúria glutárova, typ IIB $5 e $8 slo 450 $a acidúria glutárova, typ IIC $5 e $8 slo 450 $a acidúria glutárova, typ 2 $5 e $8 slo 450 $a acidémia glutárova II $5 e $8 slo 450 $a deficit FAD dehydrogenázy, mnohopočetný $5 e $8 slo 686 $a C16.320.565.100.614 686 $a C18.452.648.100.614 686 $a C18.452.660.612 750 $a Multiple Acyl Coenzyme A Dehydrogenase Deficiency $8 eng 801 -0
$a SK $b BA006 $c 20080318 801 -2
$a SK $b BA006 $c 20170111 980 $x M
Number of the records: 1