Congenital plasminogen activator inhibitor type 1 deficiency

Orpha code: 465OMIM code: 613329

Definition

A rare hemorrhagic disorder due to a constitutional haemostatic factors defect characterized by premature lysis of hemostatic clots and a moderate bleeding tendency.

Disease data
Classification

Disease

Synonyms
Congenital PAI-1 deficiency
Wrodzony Niedobór PAI-1
ORPHA code
465
OMIM code
613329
ICD10 code
D68.8
ICD11 code
3B50.1

No additional description.

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