Počet záznamov: 1
fibróza cystická
SYS d003550 LBL 00000cx--j22000003--45-- 005 20240119201211.9 100 $a 19990101csloy0103----ba0 152 $b mesh 250 $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 $8 slo 300 1-
$a 67; was PANCREATIC CYSTIC FIBROSIS 1963-66 $8 eng 330 1-
$a 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. $8 eng 450 $a Mucoviscidosis $5 e $8 eng 450 $a mukoviscidóza $5 e $8 slo 550 $3 sllk_un_auth*d019005 $Y Cystic Fibrosis Transmembrane Conductance Regulator $5 F $a regulátor vodivosti pri cystickej fibróze, transmembránový 550 $3 sllk_un_auth*d018181 $Y Mice, Inbred CFTR $5 F $a myši inbredné CFTR 550 $3 sllk_un_auth*d013546 $Y Sweating $5 B $a potenie 675 $a 616-008.6 675 $a 611.018.7 686 $a C06.689.202 686 $a C08.381.187 686 $a C16.320.190 686 $a C16.614.213 750 $a Cystic Fibrosis $8 eng 801 -0
$a US $b DNLM $c 19990101 801 -2
$a SK $b BA006 $c 20050417 820 $a a specific disease entity: do not use for fibrocystic states of various organs $8 eng 980 $x M
Počet záznamov: 1