Počet záznamov: 1  

mukopolysacharidóza II

  1. SYSd016532
    LBL
      
    00000cz--a2200000n--4500
    005
      
    20250606212851.7
    008
      
    920621|||anznnbabn-----------|-a|a------
    040
      
    $b slo $a DNLM $d BA006 $d BA006
    065
      
    $a C10.597.606.360.455.750
    065
      
    $a C16.320.322.500.750
    065
      
    $a C16.320.400.525.750
    065
      
    $a C16.320.565.202.715.645
    065
      
    $a C16.320.565.595.600.645
    065
      
    $a C17.300.550.575.645
    065
      
    $a C18.452.648.202.715.645
    065
      
    $a C18.452.648.595.600.645
    066
      
    $a 01 $c 03
    150
      
    $a mukopolysacharidóza II $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
    450
      
    $w v $a Gargoylism, Hunter Syndrome $2 eng
    450
      
    $w v $a Hunter's Syndrome $2 eng
    450
      
    $w v $a Iduronate 2-Sulfatase Deficiency $2 eng
    450
      
    $w v $a Iduronate Sulfatase Deficiency $2 eng
    450
      
    $w v $a Sulfoiduronate Sulfatase Deficiency $2 eng
    450
      
    $w v $a gargoylizmus, Hunterov syndróm $2 slo
    450
      
    $w v $a Hunterov syndróm $2 slo
    450
      
    $w v $a deficit iduronát sulfatázy $2 slo
    450
      
    $w v $a deficit iduronát-2-sulfatázy $2 slo
    450
      
    $w v $a deficit sulfoiduronát sulfatázy $2 slo
    550
      
    $7 sllk_us_auth*d007066 $Y Iduronate Sulfatase $w b $a iduronátsulfatáza
    550
      
    $7 sllk_us_auth*d008059 $Y Mucopolysaccharidosis I $w b $a mukopolysacharidóza I
    550
      
    $7 sllk_us_auth*d007066 $Y Iduronate Sulfatase $w p $a iduronátsulfatáza
    550
      
    $7 sllk_us_auth*d008059 $Y Mucopolysaccharidosis I $w p $a mukopolysacharidóza I
    665
      
    $a 1992; for MUCOPOLYSACCHARIDOSIS 2 and HUNTER'S SYNDROME use LIPOCHONDRODYSTROPHY 1976-1991 $2 eng
    665
      
    $a Mucopolysaccharidosis I (1966-1991) $2 eng
    680
    9-
    $i Systemic lysosomal storage disease marked by progressive physical deterioration and caused by a deficiency of L-sulfoiduronate sulfatase. This disease differs from MUCOPOLYSACCHARIDOSIS I by slower progression, lack of corneal clouding, and X-linked rather than autosomal recessive inheritance. The mild form produces near-normal intelligence and life span. The severe form usually causes death by age 15. $2 eng
    750
    -2
    $a Mucopolysaccharidosis II $2 eng
    980
      
    $x M
Počet záznamov: 1  

  Tieto stránky využívajú súbory cookies, ktoré uľahčujú ich prezeranie. Ďalšie informácie o tom ako používame cookies.