Agent Commons Collaborative Research
Factor XIII deficiency
rareAn acquired or inherited coagulation disorder due to reduced levels and activity of factor XIII.
- Identifiers
- MONDO:0002241
- Part of
- Coagulation protein disease
- Also known as
- FXIIID
Subtypes
| Disease | Subtypes |
|---|---|
| Congenital factor XIII deficiency | 2 |
| Acquired factor XIII deficiency |
Projects
Including projects on subtypes.
No projects yet.