A	C26692	Factor I Deficiency	Hypofibrinogenemia	Factor I Deficiency|Fibrinogen Deficiency	A usually inherited blood coagulation disorder characterized by the partial or complete absence of fibrinogen in the blood, resulting in bleeding.	Abnormally low level of fibrinogen in the blood.	C36292	Laboratory Test Result			C90259	Pediatric Terminology		
D	C98131	Hypofibrinogenemia	Hypofibrinogenemia	Factor I Deficiency|Fibrinogen Deficiency	A blood coagulation disorder characterized by low levels of fibrinogen in the blood, resulting in bleeding.	Abnormally low level of fibrinogen in the blood.	C36292	Laboratory Test Result			C90259	Pediatric Terminology		
C	C26770	Hereditary Factor XII Deficiency	Hereditary Factor XII Deficiency Disease		A rare autosomal recessive inherited bleeding disorder caused by deficiency of coagulation factor XII. It may be asymptomatic or manifest with bleeding.		C98942	Hereditary Coagulation Factor Deficiency			C90259	Pediatric Terminology		
C	C84705	Hereditary Factor XI Deficiency	Hereditary Factor XI Deficiency Disease		A rare inherited bleeding disorder caused by deficiency of coagulation factor XI. It may be asymptomatic or manifest with bleeding.		C3101	Genetic Disorder	C3093	Hemophilia	C90259	Pediatric Terminology