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congenital afibrinogenemia
Thesaurus| Noun | 1. | congenital afibrinogenemia - a rare congenital disorder of blood coagulation in which no fibrinogen is found in the blood plasmacongenital disease, genetic abnormality, genetic defect, genetic disease, genetic disorder, hereditary condition, hereditary disease, inherited disease, inherited disorder - a disease or disorder that is inherited geneticallyafibrinogenemia - the absence of fibrinogen in the plasma leading to prolonged bleeding |
EncyclopediaSeeafibrinogenemiacongenital afibrinogenemia
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. AcronymsSeecaffeinecongenital afibrinogenemia
Words related to congenital afibrinogenemianoun a rare congenital disorder of blood coagulation in which no fibrinogen is found in the blood plasmaRelated Words- congenital disease
- genetic abnormality
- genetic defect
- genetic disease
- genetic disorder
- hereditary condition
- hereditary disease
- inherited disease
- inherited disorder
- afibrinogenemia
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