/congenital afibrinogenemia

congenital afibrinogenemia

Rare Disease

MONDO:0008737

Also Known As

fibrinogen deficiencyfactor I deficiencyafibrinogenemiaafibrinogenemia congenitalafibrinogenemia, congenitalfamilial afibrinogenemiahypofibrinogenemia, congenital

Definition

Familial afibrinogenemia is a coagulation disorder characterized by bleeding symptoms due to a complete absence of circulating fibrinogen.

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Associated Genes

FGB ↗FGA ↗FGG ↗

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

Related Diseases

familial hypofibrinogenemia

MONDO:0015096

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familial hypodysfibrinogenemia

MONDO:0016638

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