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gangliozidózy
SYS d005733 LBL 00000nz--a2200000o--4500 005 20250606214720.0 008 920723|||anznnbabn-----------|-a|a------ 040 $b slo $a DNLM $d BA006 065 $a C10.228.140.163.100.435.825.300 065 $a C16.320.565.189.435.825.300 065 $a C16.320.565.398.641.803.350 065 $a C16.320.565.595.554.825.300 065 $a C18.452.132.100.435.825.300 065 $a C18.452.584.563.641.803.350 065 $a C18.452.648.189.435.825.300 065 $a C18.452.648.398.641.803.350 065 $a C18.452.648.595.554.825.300 066 $a 01 $c 03 150 $a gangliozidózy $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 $2 slo 550 $7 sllk_us_auth*d005696 $Y Galactosidases $w b $a galaktozidázy 550 $7 sllk_us_auth*d009081 $Y Mucolipidoses $w p $a mukolipidózy 550 $7 sllk_us_auth*d006596 $Y Hexosaminidases $w b $a hexozaminidázy 550 $7 sllk_us_auth*d009081 $Y Mucolipidoses $w b $a mukolipidózy 665 $a 1992(1976) $2 eng 665 $a Gangliosides (1966-1975) $2 eng 665 $a Lipoidosis (1966-1975) $2 eng 680 9-
$i A group of autosomal recessive lysosomal storage disorders marked by the accumulation of GANGLIOSIDES. They are caused by impaired enzymes or defective cofactors required for normal ganglioside degradation in the LYSOSOMES. Gangliosidoses are classified by the specific ganglioside accumulated in the defective degradation pathway. $2 eng 680 $a coordinate IM with specific ganglioside (IM) but GANGLIOSIDOSIS, GM1 and GANGLIOSIDOSES, GM2 are available $2 eng 750 -2
$a Gangliosidoses $2 eng 980 $x M
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