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fibróza cystická
SYS d003550 LBL 00000cz--a2200000o--4500 005 20250606214038.9 008 990101|||anznnbabn-----------|-a|a------ 040 $b slo $a DNLM $d BA006 065 $a C06.689.202 065 $a C08.381.187 065 $a C16.320.190 065 $a C16.614.213 066 $a 01 $c 03 089 $a 616-008.6 089 $a 611.018.7 150 $a fibróza cystická $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 Mucoviscidosis $2 eng 450 $w v $a mukoviscidóza $2 slo 550 $7 sllk_us_auth*d018181 $Y Mice, Inbred CFTR $w p $a myši inbredné CFTR 550 $7 sllk_us_auth*d019005 $Y Cystic Fibrosis Transmembrane Conductance Regulator $w p $a regulátor vodivosti pri cystickej fibróze, transmembránový 550 $7 sllk_us_auth*d013546 $Y Sweating $w b $a potenie 665 $a 67; was PANCREATIC CYSTIC FIBROSIS 1963-66 $2 eng 680 9-
$i An autosomal recessive genetic disease of the EXOCRINE GLANDS. It is caused by mutations in the gene encoding the CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR expressed in several organs including the LUNG, the PANCREAS, the BILIARY SYSTEM, and the SWEAT GLANDS. Cystic fibrosis is characterized by epithelial secretory dysfunction associated with ductal obstruction resulting in AIRWAY OBSTRUCTION; chronic RESPIRATORY INFECTIONS; PANCREATIC INSUFFICIENCY; maldigestion; salt depletion; and HEAT PROSTRATION. $2 eng 680 $a a specific disease entity: do not use for fibrocystic states of various organs $2 eng 750 -2
$a Cystic Fibrosis $2 eng 980 $x M
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