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Diseases groups

Rare thrombotic disorder due to a coagulation factors defect

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Patients organizations that work in collaboration of ERN-EuroBloodNet to improve the quality of life of patients living with diseases are included in this disease group.

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Repository of educational material produced in the ERN-EuroBloodNet focused on this disease group.

Repository of educational material produced in the ERN-EuroBloodNet focused on this disease group.

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List of the ERN-EuroBloodNet projects and links focused on this disease.

All the diseases included in this disease group are listed below!

Find further information relevant to this disease group produced by external institutions.

Education Health Professionals

Past webinars

Data standardization and linkage (Standards & Federation)

04/10/2023 12:30
Speakers: Silvia Uribe Mayoral, Vincent Planat, Davide Piscia
Target: Patients, Health professionals, Patients organizations
Subnetworks:Lymphoid malignancies, Myeloid malignancies, Red blood cell defects
Disease Groups:Transversal

Upcoming webinars

Videos

Preceptorships

Onsite trainings

Education Patients

Past webinars

PROMs and PREMs in ENROL

01/03/2023 17:00
Target: Patients
Subnetworks:Bleeding - Coagulation disorders, Bone marrow failure, Hemochromatosis and other iron disorders, Histiocytic Disorders, Lymphoid malignancies, Myeloid malignancies
Disease Groups:Transversal

Data standardization and linkage (Standards & Federation)

04/10/2023 12:30
Speakers: Silvia Uribe Mayoral, Vincent Planat, Davide Piscia
Target: Patients, Health professionals, Patients organizations
Subnetworks:Lymphoid malignancies, Myeloid malignancies, Red blood cell defects
Disease Groups:Transversal

Upcoming webinars

No entries found

Videos

Onsite trainings

Research & Publications

Observational study

Clinical trial

Publication

Diseases covered

  • Gaisböck syndrome
  • Rare thrombotic disorder due to a constitutional coagulation factors defect
  • Congenital factor XII deficiency
  • Familial thrombomodulin anomalies
  • Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency
  • Rare hereditary thrombophilia
  • Hereditary thrombophilia due to congenital protein S deficiency
  • Hereditary thrombophilia due to congenital protein C deficiency
  • Hereditary thrombophilia due to congenital antithrombin deficiency
  • Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency
  • Rare thrombotic disorder due to an acquired coagulation factors defect
  • Catastrophic antiphospholipid syndrome
  • Heparin-induced thrombocytopenia
  • Protein S acquired deficiency
  • Acquired purpura fulminans
  • Simple cryoglobulinemia