Fibrinogen deficiency, congenital: A rare congenital disorder characterized by the inability to make fibrinogen which is essential for the process of blood clotting. More detailed information about the symptoms, causes, and treatments of Fibrinogen deficiency, congenital is available below.
See full list of 13 symptoms of Fibrinogen deficiency, congenital
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Prognosis for Fibrinogen deficiency, congenital: some survive to adulthood
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Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list Fibrinogen deficiency, congenital as a "rare disease".
Source - Orphanet
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