Počet záznamov: 1
faktor XII
SYS d005174 LBL 00000cz--a2200000o--4500 005 20250606214108.1 008 990101|||anznnbabn-----------|-a|a------ 040 $b slo $a DNLM $d BA006 065 $a D08.622.500 065 $a D12.776.124.125.450 065 $a D12.776.811.243.500 065 $a D23.119.450 066 $a 01 $c 03 150 $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 $2 slo 450 $w v $a Coagulation Factor XII $2 eng 450 $w v $a Hageman Factor $2 eng 450 $w v $a faktor koagulačný XII $2 slo 450 $w v $a Hagemanov faktor $2 slo 550 $7 sllk_us_auth*d003029 $Y Coagulants $w p $a koagulanciá 550 $7 sllk_us_auth*d056828 $Y Hereditary Angioedema Type III $w p $a angioedém dedičný, typ III 550 $7 sllk_us_auth*d056828 $Y Hereditary Angioedema Type III $w b $a angioedém dedičný, typ III 665 $a 66(64) $2 eng 680 9-
$i 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. $2 eng 750 -2
$a Factor XII $2 eng 980 $x M
Počet záznamov: 1