Agent Commons Collaborative Research
Coagulation protein disease
rareCongenital or acquired deficiency of one of the coagulation factors. It results in bleeding.
- Identifiers
- MONDO:0002242
- Part of
- Blood coagulation disease
- Also known as
- coagulation factor deficiency · coagulation factor deficiency syndrome
Subtypes
Disease Rare Not rare Subtypes
- Hemophilia MONDO:0018660 17
- Von Willebrand disease (hereditary or acquired) MONDO:0024574 13
- Acquired coagulation factor deficiency MONDO:0020599 9
- Congenital fibrinogen deficiency MONDO:0018060 5
- Congenital vitamin K-dependent coagulation factors deficiency MONDO:0015722 5
- Factor XIII deficiency MONDO:0002241 4
- Combined deficiency of factor V and factor VIII MONDO:0018175 3
- Factor V deficiency MONDO:0020586 2
- Factor VII deficiency MONDO:0002244 2
- Factor X deficiency MONDO:0002247 2
- East Texas bleeding disorder MONDO:0011615
- Tatsumi factor deficiency MONDO:0010097
- Alpha-2-plasmin inhibitor deficiency MONDO:0009883 SERPINF2
- Combined deficiency of factor VII and factor X MONDO:0035776
- Congenital factor XII deficiency MONDO:0009315 F12
- Congenital high-molecular-weight kininogen deficiency MONDO:0009234 KNG1
- Congenital plasminogen activator inhibitor type 1 deficiency MONDO:0013227 SERPINE1
- Dysplasminogenemia MONDO:0100538 PLG
- Factor V amsterdam bleeding disorder MONDO:0035743
- Factor V atlanta bleeding disorder MONDO:0035759
- Factor V short isoforms-related bleeding disorder MONDO:0035742
- Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation MONDO:0015801
- Hypoplasminogenemia MONDO:0009009 PLG
- Inherited prekallikrein deficiency MONDO:0012901 KLKB1
- Multiple sclerosis-ichthyosis-factor VIII deficiency syndrome MONDO:0017837
- Plasminogen deficiency, type II MONDO:0100537 PLG
- Thrombomodulin-related bleeding disorder MONDO:0013775 THBD
- Thrombophilia due to activated protein C resistance MONDO:0008560 F5
Projects
Including projects on subtypes.
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