Severe hereditary thrombophilia due to congenital protein C deficiency

Orpha code: 745OMIM code: 176860

Definition

A rare inherited coagulation disorder characterized by deep venous thrombosis symptoms due to reduced synthesis and/or activity levels of protein C.

Disease data
Classification

Disease

Synonyms
Autosomal recessive thrombophilia due to PC deficiency
Dziedziczna trombofilia z powodu niedoboru PC
Autosomal recessive thrombophilia due to congenital protein C deficiency
ORPHA code
745
OMIM code
176860
ICD10 code
D68.2
ICD11 code
3B61.0Y

No additional description.

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