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Blood Coagulation Disorders, Inherited

Categorical breakdown of terms falling inder the category of Blood Coagulation Disorders, Inherited. Sub categories will become more specific in nature to the terms listed for Blood Coagulation Disorders, Inherited.

Sub-Categories

Terms

Activated Protein C Resistance - A hemostatic disorder characterized by a poor anticoagulant response to activated protein C (APC). T...

Afibrinogenemia - A deficiency or absence of fibrinogen (coagulation factor I) in the blood. (Dorland, 27th ed)...

Antithrombin III Deficiency - An absence or reduced level of Antithrombin III leading to an increased risk for thrombosis....

Bernard-Soulier Syndrome - A familial coagulation disorder characterized by a prolonged bleeding time, unusually large platelet...

Blood Coagulation Disorders, Inherited - Hemorrhagic and thrombotic disorders that occur as a consequence of inherited abnormalities in blood...

Factor V Deficiency - A deficiency of blood coagulation factor V (known as proaccelerin or accelerator globulin or labile ...

Factor VII Deficiency - An autosomal recessive characteristic or a coagulation disorder acquired in association with VITAMIN...

Factor X Deficiency - Blood coagulation disorder usually inherited as an autosomal recessive trait, though it can be acqui...

Factor XI Deficiency - A hereditary deficiency of blood coagulation factor XI (also known as plasma thromboplastin antecede...

Factor XII Deficiency - An absence or reduced level of blood coagulation factor XII. It normally occurs in the absence of pa...

Factor XIII Deficiency - A deficiency of blood coagulation FACTOR XIII or fibrin stabilizing factor (FSF) that prevents blood...

Hemophilia A - The classic hemophilia resulting from a deficiency of factor VIII. It is an inherited disorder of bl...

Hemophilia B - A deficiency of blood coagulation factor IX inherited as an X-linked disorder. (Also known as Christ...

Hermanski-Pudlak Syndrome - Syndrome characterized by the triad of oculocutaneous albinism (ALBINISM, OCULOCUTANEOUS); PLATELET ...

Hypoprothrombinemias - Absence or reduced levels of prothrombin in the blood....

Protein C Deficiency - An absence or deficiency in PROTEIN C which leads to impaired regulation of blood coagulation. It is...

Thrombasthenia - A congenital bleeding disorder with prolonged bleeding time, absence of aggregation of platelets in ...

von Willebrand Disease, Type 1 - A subtype of von Willebrand disease that results from a partial deficiency of VON WILLEBRAND FACTOR....

von Willebrand Disease, Type 2 - A subtype of von Willebrand disease that results from qualitative deficiencies of VON WILLEBRAND FAC...

von Willebrand Disease, Type 3 - A subtype of von Willebrand disease that results from a total or near total deficiency of VON WILLEB...

von Willebrand Diseases - Group of hemorrhagic disorders in which the VON WILLEBRAND FACTOR is either quantitatively or qualit...

Wiskott-Aldrich Syndrome - A rare, X-linked immunodeficiency syndrome characterized by ECZEMA; LYMPHOPENIA; and, recurrent pyog...