Congenital afibrinogenemia

Congenital afibrinogenemia
ICD-9	286.3

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Congenital afibrinogenemia is a rare inherited blood disorder in which the blood does not clot normally due to a lack of or a malfunction involving fibrinogen, a protein necessary for coagulation.

External links

• Online 'Mendelian Inheritance in Man' (OMIM) 202400