Severe hereditary thrombophilia due to congenital protein C deficiency

Orpha code: 745OMIM code: 176860

Definicja

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

Disease data
Klasyfikacja

Disease

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

No additional description.

Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl