Hemophilia
MONDO:0018660Hemophilia is a genetic disorder characterized by spontaneous hemorrhage or prolonged bleeding due to factor VIII or IX deficiency.
Also known as: hemophilia
217 clinical trials for this condition and its sub-types, 55 tagged with Hemophilia itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of Hemophilia
-
Hemophilia A 178 trials
5 sub-types
- Severe hemophilia A 49 trials
- Moderately severe hemophilia A 4 trials
- Mild hemophilia A 2 trials
- Hemophilia A with vascular abnormality 0 trials
- Symptomatic form of hemophilia A in female carriers 0 trials
-
Hemophilia B 84 trials · 91 incl. sub-types
4 sub-types
- Severe hemophilia B 9 trials
- Moderately severe hemophilia B 2 trials
- Mild hemophilia B 1 trial
- Symptomatic form of hemophilia B in female carriers 0 trials
-
Acquired hemophilia 2 trials · 7 incl. sub-types
3 sub-types
- Acquired hemophilia A 5 trials
- Acquired factor XI deficiency 0 trials
- Acquired hemophilia B 0 trials
-
Factor XI deficiency 0 trials
2 sub-types
- Acquired factor XI deficiency 0 trials
- Congenital factor XI deficiency 0 trials