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mukopolysacharidóza III
SYS d009084 LBL 00000nz--a2200000o--4500 005 20250606214114.4 008 921212|||anznnbabn-----------|-a|a------ 040 $b slo $a DNLM $d BA006 065 $a C16.320.565.202.715.650 065 $a C16.320.565.595.600.650 065 $a C17.300.550.575.650 065 $a C18.452.648.202.715.650 065 $a C18.452.648.595.600.650 066 $a 01 $c 03 150 $a mukopolysacharidóza III $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 Polydystrophic Oligophrenia $2 eng 450 $w v $a Sanfilippo's Syndrome $2 eng 450 $w v $a oligofrénia polydystrofická $2 slo 450 $w v $a Sanfilippov syndróm $2 slo 665 $a 92; was MUCOPOLYSACCHARIDOSIS 3 1991; was see under MUCOPOLYSACCHARIDOSIS 1975-90 $2 eng 665 $a Carbohydrate Metabolism, Inborn Errors (1966-1976) $2 eng 665 $a Mental Retardation (1966-1976) $2 eng 665 $a Mucopolysaccharides/metabolism (1966-1974) $2 eng 665 $a Mucopolysaccharidosis (1974) $2 eng 680 9-
$i Mucopolysaccharidosis characterized by heparitin sulfate in the urine, progressive mental retardation, mild dwarfism, and other skeletal disorders. There are four clinically indistinguishable but biochemically distinct forms, each due to a deficiency of a different enzyme. $2 eng 750 -2
$a Mucopolysaccharidosis III $2 eng 980 $x M
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