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Congenital afibrinogenemia
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Medical condition
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Congenital afibrinogenemia is a rare, genetically inherited blood fibrinogen disorder in which the blood does not clot normally due to the lack of fibrinogen, a blood protein necessary for coagulation. This disorder is autosomal recessive, meaning that two unaffected parents can have a child with the disorder. The lack of fibrinogen expresses...

Instance of
class of disease
Subclass of
autosomal recessive disease
Coagulopathy
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