Medical dictionary. 2011.
Congenital afibrinogenemia — Classification and external resources ICD 10 D65 ICD 9 286.3 … Wikipedia
congenital afibrinogenemia — noun a rare congenital disorder of blood coagulation in which no fibrinogen is found in the blood plasma • Hypernyms: ↑afibrinogenemia, ↑genetic disease, ↑genetic disorder, ↑genetic abnormality, ↑genetic defect, ↑congenital disease, ↑inherited… … Useful english dictionary
Afibrinogenemia — 220px Formación de fibrina durante el proceso de formación de trombos que detienen el sangrado Clasificación y recursos externos Medline … Wikipedia Español
Congenital amegakaryocytic thrombocytopenia — Classification and external resources ICD 9 287.33, 287.5 OMIM … Wikipedia
Congenital hemolytic anemia — Classification and external resources ICD 10 D55 D58 ICD 9 … Wikipedia
Congenital hypoplastic anemia — Classification and external resources ICD 10 D61.0 ICD 9 284.0 … Wikipedia
afibrinogenemia — noun the absence of fibrinogen in the plasma leading to prolonged bleeding • Hypernyms: ↑blood disease, ↑blood disorder • Hyponyms: ↑congenital afibrinogenemia * * * |āˌ noun ( s) … Useful english dictionary
congenital disease — noun a disease or disorder that is inherited genetically • Syn: ↑genetic disease, ↑genetic disorder, ↑genetic abnormality, ↑genetic defect, ↑inherited disease, ↑inherited disorder, ↑hereditary disease, ↑ … Useful english dictionary
afibrinogenemia — The absence of fibrinogen in the plasma. SEE ALSO: hypofibrinogenemia. congenital a. [MIM*202400] a rare disorder of blood coagulation in which little or no fibrinogen can be found in plasma because of a mutant … Medical dictionary
Coagulation — This article is about blood clotting. For other meanings see Coagulation (disambiguation). Coagulation is a complex process by which blood forms clots. It is an important part of hemostasis, the cessation of blood loss from a damaged vessel,… … Wikipedia
