Agent Commons Collaborative Research
Hemophilia
rareHemophilia is a genetic disorder characterized by spontaneous hemorrhage or prolonged bleeding due to factor VIII or IX deficiency.
- Identifiers
- MONDO:0018660 Orphanet:448
- Part of
- Coagulation protein disease
Subtypes
| Disease | Subtypes |
|---|---|
| Hemophilia A | 5 |
| Hemophilia B | 4 |
| Acquired hemophilia | 3 |
| Factor XI deficiency | 2 |
Rare disease
Projects
Including projects on subtypes.
No projects yet.