F7 gene related symptoms and diseases
All the information presented here about the F7 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: HGNC,ORPHANET,NCBIGENE,OMIM, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to F7 gene
Symptoms // Phenotype | % Cases |
---|---|
Bruising susceptibility | Common - Between 50% and 80% cases |
Epistaxis | Common - Between 50% and 80% cases |
Intracranial hemorrhage | Common - Between 50% and 80% cases |
Menorrhagia | Common - Between 50% and 80% cases |
Prolonged prothrombin time | Common - Between 50% and 80% cases |
Other less frequent symptoms and clinical features
Patients with F7 gene alterations may also develop some of the following symptoms and phenotypes:Commonly - More than 50% cases
- Joint hemorrhage
Not very common - Between 30% and 50% cases
- Abnormal bleeding
- Reduced factor VII activity
- Intramuscular hematoma
- Spontaneous, recurrent epistaxis
- Ecchymosis
- Hemoptysis
- Arthropathy
And 9 more phenotypes, you can get all of them using our tools for rare diseases.
Rare diseases associated to F7 gene
Here you will find a list of rare diseases related to the F7. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
CONGENITAL FACTOR VII DEFICIENCY
Alternate names
CONGENITAL FACTOR VII DEFICIENCY Is also known as congenital proconvertin deficiency, hypoproconvertinemia
Description
Factor VII (FVII) deficiency is a rare hereditary hemorrhagic disease caused by the diminution or absence of this coagulation factor.
Most common symptoms of CONGENITAL FACTOR VII DEFICIENCY
- Bruising susceptibility
- Gastrointestinal hemorrhage
- Epistaxis
- Intracranial hemorrhage
- Menorrhagia
More info about CONGENITAL FACTOR VII DEFICIENCY
SOURCES: ORPHANET
FACTOR VII DEFICIENCY
Alternate names
FACTOR VII DEFICIENCY Is also known as f7 deficiency, hypoproconvertinemia
Description
Factor VII deficiency is an autosomal recessive bleeding disorder showing variable severity (summary by Millar et al., 2000).Perry (2002) provided a comprehensive review of factor VII deficiency with a description of F7 polymorphisms, gene structure, and a summary of 120 mutations.
Most common symptoms of FACTOR VII DEFICIENCY
- Pain
- Arthritis
- Bruising susceptibility
- Abnormal bleeding
- Epistaxis
More info about FACTOR VII DEFICIENCY
SOURCES: OMIM
MYOCARDIAL INFARCTION, SUSCEPTIBILITY TO
Search interest in F7
Potential gene panels for F7 gene
F7 Sequencing Panel
By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center
This panel specifically test the F7 gene.
More info about this panelF7 Deletion/duplication analysis Panel
By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center
This panel specifically test the F7 gene.
More info about this panelF7 deficiency Panel
By Institute of Human Genetics Uniklinik RWTH Aachen
This panel specifically test the F7 gene.
More info about this panelF7. Complete sequencing Panel
By Instituto de Medicina Genomica Instituto de Medicina Genomica
This panel specifically test the F7 gene.
More info about this panelFactor VII gene sequencing Panel
By Molecular Diagnostics Laboratory University of Toledo Medical Center
This panel specifically test the F7 gene.
More info about this panelFactor VII deficiency (sequence analysis of F7 gene) Panel
By CGC Genetics
This panel specifically test the F7 gene.
More info about this panelThrombophilia FVII (p.R353Q polimorphism on F7 gene) Panel
By CGC Genetics
This panel specifically test the F7 gene.
More info about this panelBleeding Disorders Sequencing Panel with CNV Detection Panel
By PreventionGenetics PreventionGenetics Bleeding Disorders Sequencing Panel with CNV Detection that also includes the following genes: RUNX1 TBXA2R TBXAS1 VWF WAS ADAMTS13 ABCG5 ABCG8 GP6 HPS3
More info about this panelCoagulation Factor Deficiency Sequencing Panel with CNV Detection Panel
By PreventionGenetics PreventionGenetics Coagulation Factor Deficiency Sequencing Panel with CNV Detection that also includes the following genes: VWF MCFD2 VKORC1 F10 F11 F12 F13A1 F13B F2 F5
More info about this panelFactor VII Deficiency via F7 Gene Sequencing with CNV Detection Panel
By PreventionGenetics PreventionGenetics
This panel specifically test the F7 gene.
More info about this panelFactor VII deficiency Panel
By Centogene AG - the Rare Disease Company
This panel specifically test the F7 gene.
More info about this panelCentoICU platinum plus Panel
By Centogene AG - the Rare Disease Company CentoICU platinum plus that also includes the following genes: RMRP BCS1L BDNF RPS19 RPS6KA3 SALL1 SCN1A SCN2A SFTPB SFTPC
More info about this panelNew Born testing (CentoICU) Panel
By Centogene AG - the Rare Disease Company New Born testing (CentoICU) that also includes the following genes: RMRP BCS1L BDNF RPS19 RPS6KA3 SALL1 SCN1A SCN2A SFTPB SFTPC
More info about this panelF7 gene analysis Panel
By Molecular Haemostasis & Thrombosis GSTS Pathology - Guy's and St. Thomas' NHS Foundation Trust
This panel specifically test the F7 gene.
More info about this panelFactor VII deficiency Panel
By Molecular Haemostasis & Thrombosis GSTS Pathology - Guy's and St. Thomas' NHS Foundation Trust
This panel specifically test the F7 gene.
More info about this panelFactor VII Deficiency Panel
By Medical Genetics Laboratory Bambino Gesù Children's Hospital
This panel specifically test the F7 gene.
More info about this panelFactor VII Deficiency (F7) Panel
By MVZ Dortmund Dr. Eberhard & Partner
This panel specifically test the F7 gene.
More info about this panelFactor VII Deficiency Panel
By Labor-MVZ Westmecklenburg Laboratory for Molecular Diagnostics
This panel specifically test the F7 gene.
More info about this panelaCGH Deletion/Duplication Analysis Panel
By BloodCenter of Wisconsin Diagnostic Laboratories BloodCenter of Wisconsin, part of Versiti aCGH Deletion/Duplication Analysis that also includes the following genes: CFB RUNX1 STXBP2 TBXA2R THBD VWF WAS C3 C4BPA C4BPB
More info about this panelFactor VII deficiency Panel
By Praxis fuer Humangenetik Wien
This panel specifically test the F7 gene.
More info about this panelFactor 7 deficiency Panel
By Regional Molecular Haemostasis Laboratory Birmingham Childrens Hospital NHS Foundation Trust
This panel specifically test the F7 gene.
More info about this panelFactor VII deficiency Panel
By MedGene
This panel specifically test the F7 gene.
More info about this panelFactor VII Panel
By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
This panel specifically test the F7 gene.
More info about this panelF7 Panel
By Fulgent Genetics Fulgent Genetics
This panel specifically test the F7 gene.
More info about this panelBleeding Disorder/Coagulopathy Panel Panel
By Blueprint Genetics Bleeding Disorder/Coagulopathy Panel that also includes the following genes: RUNX1 SRC TBXA2R THBD VWF WAS ADAMTS13 ABCG5 ABCG8 HPS3
More info about this panelCoagulation Factor Deficiency Panel Panel
By Blueprint Genetics Coagulation Factor Deficiency Panel that also includes the following genes: VWF VKORC1 F10 F11 F12 F13A1 F2 F5 F7 F8
More info about this panelComprehensive Hematology Panel Panel
By Blueprint Genetics Comprehensive Hematology Panel that also includes the following genes: RHAG RIT1 RPL11 RPL15 RPL35A RPL5 RPS10 RPS19 RPS24 RPS26
More info about this panelCongenital factor VII deficiency Panel
By Bioarray
This panel specifically test the F7 gene.
More info about this panelFACTOR VII DEFICIENCY (HYPOPROCONVERTINEMIA) Panel
By Laboratorio de Genetica Clinica SL
This panel specifically test the F7 gene.
More info about this panelCongenital Factor VII Deficiency, Sequencing F7 Gene Panel
By Reference Laboratory Genetics
This panel specifically test the F7 gene.
More info about this panelBleeding Disorders , Panel Massive Sequencing (NGS) 23 Genes Panel
By Reference Laboratory Genetics Bleeding Disorders , Panel Massive Sequencing (NGS) 23 Genes that also includes the following genes: VWF ADAMTS13 MCFD2 F10 F11 F12 F13A1 F2 F5 F7
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