Factor Xii Deficiency (FA12D)

Alias:
Hageman Factor Deficiency
Factor Xii Deficiency Disease
Haf Deficiency
Deficiency, Factor Xii
Deficiency, Hageman
F12 Deficiency
Factor Xii
Fa12d
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Factor Xii Deficiency, also known as hageman factor deficiency, is related to congenital factor xii deficiency and angioedema, hereditary, 3. An important gene associated with Factor Xii Deficiency is F12 (Coagulation Factor XII), and among its related pathways/superpathways are Response to elevated platelet cytosolic Ca2+ and Diseases of hemostasis. The drugs Kallikreins and Sodium citrate have been mentioned in the context of this disorder. Affiliated tissues include whole blood and brain, and related phenotypes are prolonged partial thromboplastin time and reduced factor xii activity
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
All ages
--
14
102
31

Medical Symptom

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Description
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HPO Source Accession
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Gene & Mutation

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Mutations
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Disease Model

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Name
MGI
Related Gene
Strain of Origin
Publications
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References Literature

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