Severe hereditary thrombophilia due to congenital protein S deficiency

Orpha code: 743OMIM code: 614514

Definition

An inherited coagulation disorder characterized by recurrent venous thrombosis symptoms due to reduced synthesis and/or activity levels of protein S.

Disease data
Classification

Disease

Synonyms
Autosomal recessive thrombophilia due to congenital protein S deficiency
ORPHA code
743
OMIM code
614514
ICD10 code
D68.5
ICD11 code
3B61.0Y

No additional description.

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