F10 gene related symptoms and diseases
All the information presented here about the F10 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: NCBIGENE,OMIM,ORPHANET,HGNC, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to F10 gene
Symptoms // Phenotype | % Cases |
---|---|
Respiratory tract infection | Very Common - Between 80% and 100% cases |
Arthropathy | Very Common - Between 80% and 100% cases |
Lupus anticoagulant | Very Common - Between 80% and 100% cases |
Intramuscular hematoma | Very Common - Between 80% and 100% cases |
Antiphospholipid antibody positivity | Very Common - Between 80% and 100% cases |
Other less frequent symptoms and clinical features
Patients with F10 gene alterations may also develop some of the following symptoms and phenotypes:Commonly - More than 50% cases
- Spontaneous hematomas
- Joint hemorrhage
- Prolonged prothrombin time
- Prolonged partial thromboplastin time
- Gingival bleeding
- Amyloidosis
- Abnormality of the musculature
- Abnormality of the liver
And 10 more phenotypes, you can get all of them using our tools for rare diseases.
Rare diseases associated to F10 gene
Here you will find a list of rare diseases related to the F10. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
CONGENITAL FACTOR X DEFICIENCY
Alternate names
CONGENITAL FACTOR X DEFICIENCY Is also known as f10 deficiency, congenital stuart factor deficiency, stuart-prower factor deficiency
Description
Congenital factor X deficiency is an inherited bleeding disorder with a decreased antigen and/or activity of factor X (FX) and characterized by mild to severe bleeding symptoms.
Most common symptoms of CONGENITAL FACTOR X DEFICIENCY
- Respiratory tract infection
- Abnormality of the liver
- Bruising susceptibility
- Hematuria
- Abnormal bleeding
More info about CONGENITAL FACTOR X DEFICIENCY
Search interest in F10
Potential gene panels for F10 gene
FX deficiency Panel
By Institute of Human Genetics Uniklinik RWTH Aachen
This panel specifically test the F10 gene.
More info about this panelHereditary amyloidosis (NGS panel of 19 genes) Panel
By CGC Genetics Hereditary amyloidosis (NGS panel of 19 genes) that also includes the following genes: TACSTD2 TGFBI TNFRSF1A TTR NLRP3 IL31RA CST3 F10 FGA GSN
More info about this panelCongenital factor X deficiency (sequence analysis of F10 gene) Panel
By CGC Genetics
This panel specifically test the F10 gene.
More info about this panelHereditary amyloidosis (NGS panel of 19 genes) Panel
By CGC Genetics Hereditary amyloidosis (NGS panel of 19 genes) that also includes the following genes: TACSTD2 TGFBI TNFRSF1A TTR NLRP3 IL31RA CST3 F10 FGA GSN
More info about this panelCongenital factor X deficiency (sequence analysis of F10 gene) Panel
By CGC Genetics
This panel specifically test the F10 gene.
More info about this panelFactor X Deficiency via F10 Gene Sequencing with CNV Detection Panel
By PreventionGenetics PreventionGenetics
This panel specifically test the F10 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 10 Deficiency Panel
By GeneTech ATS GeneTech Private Limited
This panel specifically test the F10 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 panelFactor X gene analysis Panel
By Molecular Haemostasis & Thrombosis GSTS Pathology - Guy's and St. Thomas' NHS Foundation Trust
This panel specifically test the F10 gene.
More info about this panelFactor X Deficiency Panel
By Medical Genetics Laboratory Bambino Gesù Children's Hospital
This panel specifically test the F10 gene.
More info about this panelPlatelets, Coagulation disorders Panel Panel
By CeGaT GmbH Platelets, Coagulation disorders Panel that also includes the following genes: VHL VWF ADAMTS13 TET2 DSG1 ENTPD1 ETV6 F10 F11 F12
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 10 deficiency Panel
By Praxis fuer Humangenetik Wien
This panel specifically test the F10 gene.
More info about this panelFactor X Deficiency Panel
By Regional Molecular Haemostasis Laboratory Birmingham Childrens Hospital NHS Foundation Trust
This panel specifically test the F10 gene.
More info about this panelFactor 10 deficiency Panel
By MedGene
This panel specifically test the F10 gene.
More info about this panelF10 Panel
By Fulgent Genetics Fulgent Genetics
This panel specifically test the F10 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 panelAMYLOIDOSIS HEREDITARY NGS PANEL Panel
By Laboratorio de Genetica Clinica SL AMYLOIDOSIS HEREDITARY NGS PANEL that also includes the following genes: TACSTD2 TGFBI TNFRSF1A TTR NLRP3 IL31RA CST3 F10 FGA GSN
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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