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. The following codes are used with International Statistical Classification of Diseases and Related Health Problems. ... The following is a list of codes for International Statistical Classification of Diseases and Related Health Problems. ... Human blood smear: a - erythrocytes; b - neutrophil; c - eosinophil; d - lymphocyte. ... Fibrin is a protein involved in the clotting of blood. ... A representation of the 3D structure of myoglobin, showing coloured alpha helices. ... The coagulation of blood is a complex process during which blood forms solid clots. ...
Afibrinogenemia and hypofibrinogenemia result from mutations that affect plasma fibrinogen concentration and are frequently associated with a bleeding diathesis.
Afibrinogenemia is autosomal recessive, with a male-to-female ratio of 1:1.
Afibrinogenemia is often first diagnosed in the newborn period because of umbilical cord bleeding.
Congenital Afibrinogenemia is a rare disorder characterized by absence of a certain substance (protein) in the blood that is essential in the blood clotting (coagulation) process.
Congenital Afibrinogenemia is thought to be transmitted as an autosomal recessive trait.
Congenital Afibrinogenemia is a very rare blood disorder in which the patient is born with little or no fibrinogen in the circulating blood.
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