Factor Xi Deficiency (FA11D)

Alias:

Plasma Thromboplastin Antecedent Deficiency

Rosenthal Syndrome

Rosenthal Factor Deficiency

Pta Deficiency

Hemophilia C

Hereditary Factor Xi Deficiency Disease

Congenital Factor Xi Deficiency

F11 Deficiency

Haemophilia C

Factor Xi Deficiency, Autosomal Dominant

Factor 11 Deficiency

Rosenthal's Disease

Pta - [plasma Thromboplastin Antecedent] Deficiency

Factor Xi Deficiency, Autosomal Recessive

Congenital Factor Xi Deficiency Disease

Thromboplastin Antecedent Deficiency

Factor Xi Deficiency, Congenital

Facotr Xi Deficiency

Rosenthal Disease

Factor Xi

Fa11d

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Factor Xi Deficiency, also known as plasma thromboplastin antecedent deficiency, is related to hemophilia and vitamin k deficiency bleeding. An important gene associated with Factor Xi Deficiency is F11 (Coagulation Factor XI), and among its related pathways/superpathways are Infectious disease and Response to elevated platelet cytosolic Ca2+. The drugs Heparin, bovine and Apixaban have been mentioned in the context of this disorder. Affiliated tissues include skin and liver, and related phenotypes are abnormal bleeding and reduced factor xi activity

Related ID：

MALACARDS：FCT002

OMIM：612416

MESH：D005173

ICD11：413739466