Hereditary thrombophilia due to congenital protein S deficiency

rare

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

Identifiers: MONDO:0019144 Orphanet:743
Part of: Inherited thrombophilia Protein S deficiency
Also known as: autosomal recessive thrombophilia due to congenital protein S deficiency

Subtypes

All diseases Rare only

Disease	ID	Subtypes	Genes
Thrombophilia due to protein S deficiency, autosomal dominant	MONDO:0012868		PROS1
Thrombophilia due to protein S deficiency, autosomal recessive	MONDO:0013791		PROS1

Rare disease

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