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thrombophilia due to protein C deficiency, autosomal recessive

Disease Summary
Associated Targets (1)
Tchem

1


GARD Rare
Uniprot Description A hemostatic disorder characterized by impaired regulation of blood coagulation and a tendency to recurrent venous thrombosis. It results in a thrombotic condition that can manifest as a severe neonatal disorder or as a milder disorder with late-onset thrombophilia. The severe form leads to neonatal death through massive neonatal venous thrombosis. Often associated with ecchymotic skin lesions which can turn necrotic called purpura fulminans, this disorder is very rare.
Mondo Term and Equivalent IDs
MONDO:0012860:  thrombophilia due to protein C deficiency, autosomal recessive
GARD:0013041: 
MESH:C567353: 
UMLS:C2676759: