congenital afibrinogenemia


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con·gen·i·tal a·fi·brin·o·gen·e·mi·a

[MIM*202400]
a rare disorder of blood coagulation in which little or no fibrinogen can be found in plasma because of a mutant form in one of the three fibrinogen loci. Leads to defective platelet aggregation; autosomal recessive inheritance.

con·gen·i·tal a·fi·brin·o·gen·e·mi·a

(kŏn-jen'i-tăl ā-fī'brin-ō-jĕ-nē'mē-ă)
A rare disorder of blood coagulation in which little or no fibrinogen can be detected in plasma.
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