Congenital alpha2-antiplasmin deficiency

Orpha code: 79OMIM code: 262850

Definition

A rare hemorrhagic disorder caused by congenital deficiency of alpha2 antiplasmin, leading to dysregulated fibrinolysis and is characterized by a hemorrhagic tendency presenting from childhood with prolonged bleeding and ecchymoses following minor trauma and spontaneous bleeding episodes (often in unusual locations like diaphysis of long bones).

Disease data
Classification

Disease

ORPHA code
79
OMIM code
262850
ICD10 code
D68.8
ICD11 code
3B50.0

No additional description.

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