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ENFactor X Deficiency (FA10D)
Alias:
Stuart-Prower Factor Deficiency
Congenital Stuart Factor Deficiency
Congenital Factor X Deficiency
F10 Deficiency
Hereditary Factor X Deficiency Disease
Stuart Factor Deficiency, Congenital
Factor X Deficiency, Congenital
Stuart Deficiency Disease
Stuart Prower Deficiency
Disease, Stuart-Prower
Deficiency of Factor X
Stuart-Prower Disease
Factor 10 Deficiency
Deficiency, Factor X
Fa10d
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Factor X Deficiency, also known as stuart-prower factor deficiency, is related to prothrombin deficiency, congenital and vitamin k deficiency bleeding. An important gene associated with Factor X Deficiency is F10 (Coagulation Factor X), and among its related pathways/superpathways are Metabolism of proteins and Response to elevated platelet cytosolic Ca2+. Affiliated tissues include liver and skin, and related phenotypes are prolonged prothrombin time and reduced factor x activity
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MALACARDS
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