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mukopolysacharidózy
SYS d009083 LBL 00000nz--a2200000o--4500 005 20250606213020.7 008 990101|||anznnbabn-----------|-a|a------ 040 $b slo $a DNLM $d BA006 065 $a C16.320.565.202.715 065 $a C16.320.565.595.600 065 $a C17.300.550.575 065 $a C18.452.648.202.715 065 $a C18.452.648.595.600 066 $a 01 $c 03 150 $a mukopolysacharidózy $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 665 $a 92; was MUCOPOLYSACCHARIDOSIS 1974-91 $2 eng 680 9-
$i Group of lysosomal storage diseases each caused by an inherited deficiency of an enzyme involved in the degradation of glycosaminoglycans (mucopolysaccharides). The diseases are progressive and often display a wide spectrum of clinical severity within one enzyme deficiency. $2 eng 680 $a lysosomal storage dis; types I through VII except V are available as main headings: V = MUCOPOLYSACCHARIDOSIS V see MUCOPOLYSACCHARIDOSIS I; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES $2 eng 750 -2
$a Mucopolysaccharidoses $2 eng 980 $x M
Počet záznamov: 1