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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.