congenital afibrinogenemia
Noun
-
A rare congenital disorder of blood coagulation in which no fibrinogen is found in the blood plasma (synset 114194974)
is a type of:
- congenital disease, genetic abnormality, genetic defect, genetic disease, genetic disorder, hereditary condition, hereditary disease, inherited disease, inherited disorder - a disease or disorder that is inherited genetically
- afibrinogenemia - the absence of fibrinogen in the plasma leading to prolonged bleeding
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