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
Part of
Blood coagulation disease
Also known as
coagulation factor deficiency · coagulation factor deficiency syndrome

Subtypes

All diseases Rare only
Disease Subtypes
Hemophilia 17
Von Willebrand disease (hereditary or acquired) 13
Acquired coagulation factor deficiency 9
Congenital fibrinogen deficiency 5
Congenital vitamin K-dependent coagulation factors deficiency 5
Factor XIII deficiency 4
Combined deficiency of factor V and factor VIII 3
Factor V deficiency 2
Factor VII deficiency 2
Factor X deficiency 2
East Texas bleeding disorder
Tatsumi factor deficiency
Alpha-2-plasmin inhibitor deficiency
Combined deficiency of factor VII and factor X
Congenital factor XII deficiency
Congenital high-molecular-weight kininogen deficiency
Congenital plasminogen activator inhibitor type 1 deficiency
Dysplasminogenemia
Factor V amsterdam bleeding disorder
Factor V atlanta bleeding disorder
Factor V short isoforms-related bleeding disorder
Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation
Hypoplasminogenemia
Inherited prekallikrein deficiency
Multiple sclerosis-ichthyosis-factor VIII deficiency syndrome
Plasminogen deficiency, type II
Thrombomodulin-related bleeding disorder
Thrombophilia due to activated protein C resistance

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