KEGG   DISEASE: プラスミノーゲン活性化因子インヒビター1欠損症
エントリ  
H01106                                                             
名称    
プラスミノーゲン活性化因子インヒビター1欠損症
概要    
Plasminogen activator inhibitor type 1 (PAI-1) deficiency is a disorder resulting in increased fibrinolysis and an associated bleeding diathesis. PAI-1 is an important component of the coagulation system that down-regulates fibrinolysis in the circulation. Affected individuals exhibit mild to moderate bleeding symptoms, including epistaxis, menorrhagia, and delayed bleeding after trauma or surgical procedures. Spontaneous bleeding events are rarely seen in contrast to other procoagulant deficiencies. Generally most of the PAI-1-related diseases are due to elevated antigenic concentrations and their inhibitory activity. However, absence of cellular PAI-1 activity also causes several diseases. Clear documentation of PAI-1 deficiency as a cause of a bleeding disorder has been rare.
カテゴリ  
血液疾患
階層分類  
ICD-11 による疾患分類 [BR:jp08403]
 03 血液・造血器の疾患
  凝固障害, 紫斑病またはその他の出血性または関連病状
   線維素溶解障害
    3B50  先天性線維素溶解障害
     H01106  プラスミノーゲン活性化因子インヒビター1欠損症
パスウェイに基づく疾患分類 [BR:jp08402]
 免疫系
  nt06514  凝固カスケード
   H01106  プラスミノーゲン活性化因子インヒビター1欠損症
パスウェイ 
hsa04610  Complement and coagulation cascades
ネットワーク
nt06514 Coagulation cascade
病因遺伝子 
PAI1 [HSA:5054] [KO:K03982]
リンク   
ICD-11: 3B50.1
MeSH: C567640
OMIM: 613329
文献    
  著者
Mehta R, Shapiro AD
  タイトル
Plasminogen activator inhibitor type 1 deficiency.
  雑誌
Haemophilia 14:1255-60 (2008)
DOI:10.1111/j.1365-2516.2008.01834.x
文献    
  著者
Ghosh AK, Vaughan DE
  タイトル
PAI-1 in tissue fibrosis.
  雑誌
J Cell Physiol 227:493-507 (2012)
DOI:10.1002/jcp.22783
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