Congenital Disorder

Blood Coagulation Disorders, Inherited

AMW:DIS:150041

Hemorrhagic and thrombotic disorders that occur as a consequence of inherited abnormalities in blood coagulation.

Pathology clinical

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Blood Coagulation Disorders, Inherited has parent Blood Coagulation Disorders

Hermanski-Pudlak Syndrome has parent Blood Coagulation Disorders, Inherited

Activated Protein C Resistance has parent Blood Coagulation Disorders, Inherited

Afibrinogenemia has parent Blood Coagulation Disorders, Inherited

Antithrombin III Deficiency has parent Blood Coagulation Disorders, Inherited

Bernard-Soulier Syndrome has parent Blood Coagulation Disorders, Inherited

Factor V Deficiency has parent Blood Coagulation Disorders, Inherited

Factor VII Deficiency has parent Blood Coagulation Disorders, Inherited

Factor X Deficiency has parent Blood Coagulation Disorders, Inherited

Factor XI Deficiency has parent Blood Coagulation Disorders, Inherited

Factor XII Deficiency has parent Blood Coagulation Disorders, Inherited

Factor XIII Deficiency has parent Blood Coagulation Disorders, Inherited

Hemophilia A has parent Blood Coagulation Disorders, Inherited

Hemophilia B has parent Blood Coagulation Disorders, Inherited

Hypoprothrombinemias has parent Blood Coagulation Disorders, Inherited

Protein C Deficiency has parent Blood Coagulation Disorders, Inherited

Thrombasthenia has parent Blood Coagulation Disorders, Inherited

von Willebrand Diseases has parent Blood Coagulation Disorders, Inherited

Wiskott-Aldrich Syndrome has parent Blood Coagulation Disorders, Inherited

Gray Platelet Syndrome has parent Blood Coagulation Disorders, Inherited

Blood Coagulation Disorders, Inherited has parent Genetic Diseases, Inborn

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