Factor Vii Deficiency (FA7D)

Alias:
Hypoproconvertinemia
Congenital Factor Vii Deficiency
Congenital Proconvertin Deficiency
F7 Deficiency
Serum Prothrombin Conversion Accelerator Deficiency
Prothrombin Conversion Accelerator Deficiency
Proconvertin Deficiency, Congenital
Proconvertin Deficiency
Deficiency, Factor Vii
Factor 7 Deficiency
Deficiency, Stable
Stable Disease
Fa7d
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Factor Vii Deficiency, also known as hypoproconvertinemia, is related to vitamin k deficiency bleeding and hemophilia, and has symptoms including epistaxis An important gene associated with Factor Vii Deficiency is F7 (Coagulation Factor VII), and among its related pathways/superpathways are Response to elevated platelet cytosolic Ca2+ and PI3K-Akt signaling pathway. The drugs Ofatumumab and Sorafenib have been mentioned in the context of this disorder. Affiliated tissues include Liver and lung, and related phenotypes are gastrointestinal hemorrhage and intracranial hemorrhage
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
AD
All ages
1-9/1000000
13
125
77

Medical Symptom

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

Gene & Mutation

#
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
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