Number of the records: 1
faktor XII
SYS d005174 LBL 00000cx--j22000003--45-- 005 20240119201506.1 100 $a 19990101csloy0103----ba0 152 $b mesh 250 $a faktor XII $x AD $x AE $x AG $x AI $x AN $x BI $x CF $x CH $x CL $x CS $x DE $x EC $x GE $x HI $x IM $x IP $x ME $x PD $x PH $x PK $x PO $x RE $x SD $x ST $x TO $x TU $x UL $x UR $8 slo 300 1-
$a 66(64) $8 eng 330 1-
$a Stable blood coagulation factor activated by contact with the subendothelial surface of an injured vessel. Along with prekallikrein, it serves as the contact factor that initiates the intrinsic pathway of blood coagulation. Kallikrein activates factor XII to XIIa. Deficiency of factor XII, also called the Hageman trait, leads to increased incidence of thromboembolic disease. Mutations in the gene for factor XII that appear to increase factor XII amidolytic activity are associated with HEREDITARY ANGIOEDEMA TYPE III. $8 eng 450 $a Coagulation Factor XII $5 e $8 eng 450 $a Hageman Factor $5 e $8 eng 450 $a faktor koagulačný XII $5 e $8 slo 450 $a Hagemanov faktor $5 e $8 slo 550 $3 sllk_un_auth*d003029 $Y Coagulants $5 F $a koagulanciá 550 $3 sllk_un_auth*d056828 $Y Hereditary Angioedema Type III $5 F $a angioedém dedičný, typ III 550 $3 sllk_un_auth*d056828 $Y Hereditary Angioedema Type III $5 B $a angioedém dedičný, typ III 686 $a D08.622.500 686 $a D12.776.124.125.450 686 $a D12.776.811.243.500 686 $a D23.119.450 750 $a Factor XII $8 eng 801 -0
$a US $b DNLM $c 19990101 801 -2
$a SK $b BA006 $c 20030212 980 $x M
Number of the records: 1