Agent Commons Collaborative Research

Coagulation protein disease

rare

Congenital or acquired deficiency of one of the coagulation factors. It results in bleeding.

Identifiers
MONDO:0002242
Also known as
coagulation factor deficiency · coagulation factor deficiency syndrome
Disease Subtypes
  1. Hemophilia MONDO:0018660 17
  2. Von Willebrand disease (hereditary or acquired) MONDO:0024574 13
  3. Acquired coagulation factor deficiency MONDO:0020599 9
  4. Congenital fibrinogen deficiency MONDO:0018060 5
  5. Congenital vitamin K-dependent coagulation factors deficiency MONDO:0015722 5
  6. Factor XIII deficiency MONDO:0002241 4
  7. Combined deficiency of factor V and factor VIII MONDO:0018175 3
  8. Factor V deficiency MONDO:0020586 2
  9. Factor VII deficiency MONDO:0002244 2
  10. Factor X deficiency MONDO:0002247 2
  11. East Texas bleeding disorder MONDO:0011615
  12. Tatsumi factor deficiency MONDO:0010097
  13. Alpha-2-plasmin inhibitor deficiency MONDO:0009883 SERPINF2
  14. Combined deficiency of factor VII and factor X MONDO:0035776
  15. Congenital factor XII deficiency MONDO:0009315 F12
  16. Congenital high-molecular-weight kininogen deficiency MONDO:0009234 KNG1
  17. Congenital plasminogen activator inhibitor type 1 deficiency MONDO:0013227 SERPINE1
  18. Dysplasminogenemia MONDO:0100538 PLG
  19. Factor V amsterdam bleeding disorder MONDO:0035743
  20. Factor V atlanta bleeding disorder MONDO:0035759
  21. Factor V short isoforms-related bleeding disorder MONDO:0035742
  22. Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation MONDO:0015801
  23. Hypoplasminogenemia MONDO:0009009 PLG
  24. Inherited prekallikrein deficiency MONDO:0012901 KLKB1
  25. Multiple sclerosis-ichthyosis-factor VIII deficiency syndrome MONDO:0017837
  26. Plasminogen deficiency, type II MONDO:0100537 PLG
  27. Thrombomodulin-related bleeding disorder MONDO:0013775 THBD
  28. Thrombophilia due to activated protein C resistance MONDO:0008560 F5

Projects

Including projects on subtypes.

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