Number of the records: 1
glykogenóza, typ I
SYS d005953 LBL 00000cx--j2200000---45-- 005 20240119195659.0 100 $a 19990101asloy0103----ba0 152 $b mesh 250 $a glykogenóza, typ I $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 1989; use GLUCOSEPHOSPHATASE DEFICIENCY 1964-1988; for VON GIERKE'S DISEASE use GLYCOGENOSIS 1963-1964 $8 eng 330 1-
$a An autosomal recessive disease in which gene expression of glucose-6-phosphatase is absent, resulting in hypoglycemia due to lack of glucose production. Accumulation of glycogen in liver and kidney leads to organomegaly, particularly massive hepatomegaly. Increased concentrations of lactic acid and hyperlipidemia appear in the plasma. Clinical gout often appears in early childhood. $8 eng 450 $a Glucose-6-Phosphatase Deficiency $5 e $8 eng 450 $a Glucosephosphatase Deficiency $5 e $8 eng 450 $a Glycogenosis 1 $5 e $8 eng 450 $a Hepatorenal Glycogen Storage Disease $5 e $8 eng 450 $a von Gierke Disease $5 e $8 eng 450 $a choroba z ukladania glykogénu, typ I $5 e $8 slo 450 $a deficit glukóza-6-fosfatázy $5 e $8 slo 450 $a deficit glukózafosfatázy $5 e $8 slo 450 $a glykogenóza 1 $5 e $8 slo 450 $a choroba z ukladania glykogénu, hepatorenálna $5 e $8 slo 450 $a glykogenóza hepatorenálna $5 e $8 slo 450 $a von Gierkeho choroba $5 e $8 slo 686 $a C16.320.565.202.449.448 686 $a C18.452.648.202.449.448 750 $a Glycogen Storage Disease Type I $8 eng 801 -0
$a US $b DNLM $c 19990101 801 -2
$a SK $b BA006 $c 20020319 801 -2
$a SK $b BA006 $c 20090716 820 $a do not use /congen & do not coord with INFANT, NEWBORN, DISEASES $8 eng 980 $x M
Number of the records: 1