coagulation protein disease
MONDO:0002242Mondo
Findings
No curated finding names coagulation protein disease yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Congenital or acquired deficiency of one of the coagulation factors. It results in bleeding.
Definition from the Mondo Disease Ontology (MONDO:0002242), read 2026-09-29. CC BY 4.0.
Where it sits
- A kind of
- Narrower terms (28)
- acquired coagulation factor deficiency
- alpha-2-plasmin inhibitor deficiency
- combined deficiency of factor V and factor VIII
- combined deficiency of factor VII and factor X
- congenital factor XII deficiency
- congenital fibrinogen deficiency
- congenital high-molecular-weight kininogen deficiency
- congenital plasminogen activator inhibitor type 1 deficiency
- congenital vitamin K-dependent coagulation factors deficiency
- dysplasminogenemia
- East Texas bleeding disorder
- factor V amsterdam bleeding disorder
- factor V atlanta bleeding disorder
- factor V deficiency
- factor V short isoforms-related bleeding disorder
- factor VII deficiency
- factor X deficiency
- factor XIII deficiency
- hemophilia
- hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation
- hypoplasminogenemia
- inherited prekallikrein deficiency
- multiple sclerosis-ichthyosis-factor VIII deficiency syndrome
- plasminogen deficiency, type II
- Tatsumi factor deficiency
- thrombomodulin-related bleeding disorder
- thrombophilia due to activated protein C resistance
- von Willebrand disease (hereditary or acquired)
Other names
2 names
Resolves to: coagulation protein disease
- Also called
- coagulation factor deficiencycoagulation factor deficiency syndrome