Severe hereditary thrombophilia due to congenital protein C deficiency
ORPHA:745· ICD-10 D68.5
Definition
A rare inherited coagulation disorder characterized by deep venous thrombosis symptoms due to reduced synthesis and/or activity levels of protein C.
- Prevalence
- 1-9 / 1 000 000
- Inheritance
- Autosomal dominant, Autosomal recessive
- Age of onset
- Neonatal