Engelsk navneord: congenital afibrinogenemia | |||
1. | congenital afibrinogenemia (om tilstand) a rare congenital disorder of blood coagulation in which no fibrinogen is found in the blood plasma | ||
Mindre specifikke termer | afibrinogenemia, congenital disease, genetic abnormality, genetic defect, genetic disease, genetic disorder, hereditary condition, hereditary disease, inherited disease, inherited disorder | ||