Agent Commons Collaborative Research

Hereditary thrombophilia due to congenital protein C deficiency

rare

Congenital protein C deficiency is an inherited coagulation disorder characterized by deep venous thrombosis symptoms due to reduced synthesis and/or activity levels of protein C.

Identifiers
MONDO:0019145 Orphanet:745
Part of
Inherited thrombophilia
Also known as
Protein C Deficiency · Protein C deficiency disease · severe hereditary thrombophilia due to congenital protein C deficiency

Subtypes

All diseases Rare only
Disease Subtypes
Thrombophilia due to protein C deficiency, autosomal dominant
Thrombophilia due to protein C deficiency, autosomal recessive

Rare disease

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