Severe hereditary thrombophilia due to congenital protein S deficiency
ORPHA:743· ICD-10 D68.5
Definition
An inherited coagulation disorder characterized by recurrent venous thrombosis symptoms due to reduced synthesis and/or activity levels of protein S.
- Prevalence
- Unknown
- Inheritance
- Autosomal recessive
- Age of onset
- Infancy, Neonatal