Prothrombin Deficiency

Alias:
Factor Ii Deficiency
Hypoprothrombinemia
Dysprothrombinemia
Congenital Factor Ii Deficiency
Hereditary Factor Ii Deficiency Disease
Inherited Factor Ii Deficiency
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Prothrombin Deficiency, also known as factor ii deficiency, is related to prothrombin deficiency, congenital and infective endocarditis. An important gene associated with Prothrombin Deficiency is F2 (Coagulation Factor II, Thrombin), and among its related pathways/superpathways are Metabolism of proteins and Response to elevated platelet cytosolic Ca2+. The drugs Warfarin and Anticoagulants have been mentioned in the context of this disorder. Affiliated tissues include liver and brain, and related phenotypes are prolonged prothrombin time and prolonged partial thromboplastin time
Related ID:
MESH:C562724

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
All ages
<1/1000000
11
76
20

Medical Symptom

#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Gene
Function
Score
Mutations
No data available

Related Drugs

Name
CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

Title
PMID
Journal
Year
IF
No Data Found!
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