Factor Xiii Deficiency

Alias:
Hereditary Factor Xiii Deficiency Disease
Deficiency, Laki-Lorand Factor
Fibrin Stabilizing Factor Deficiency
Factor Xiii Deficiency Disease
Deficiency of Factor Xiii
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Factor Xiii Deficiency, also known as hereditary factor xiii deficiency disease, is related to congenital factor xiii deficiency and purpura, and has symptoms including prolonged umbilical cord bleeding An important gene associated with Factor Xiii Deficiency is F13A1 (Coagulation Factor XIII A Chain), and among its related pathways/superpathways are Response to elevated platelet cytosolic Ca2+ and Collagen chain trimerization. The drugs Benzocaine and Tannic acid have been mentioned in the context of this disorder. Affiliated tissues include placenta and whole blood, and related phenotypes are homeostasis/metabolism and mortality/aging
Related ID:
MESH:D005177

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
All ages
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11
89
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Medical Symptom

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Gene & Mutation

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Disease Model

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MGI
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Publications
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References Literature

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