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.

Mendelian

Accelerate your rare disease diagnosis with us

Learn more

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

SOURCES: OMIM ORPHANET


Potential gene panels for F10 gene

FX deficiency Panel

Germany.

By Institute of Human Genetics Uniklinik RWTH Aachen

This panel specifically test the F10 gene.

More info about this panel

Hereditary amyloidosis (NGS panel of 19 genes) Panel

Portugal.

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 panel

Congenital factor X deficiency (sequence analysis of F10 gene) Panel

Portugal.

By CGC Genetics

This panel specifically test the F10 gene.

More info about this panel

Hereditary amyloidosis (NGS panel of 19 genes) Panel

Portugal.

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 panel

Congenital factor X deficiency (sequence analysis of F10 gene) Panel

Portugal.

By CGC Genetics

This panel specifically test the F10 gene.

More info about this panel

Factor X Deficiency via F10 Gene Sequencing with CNV Detection Panel

United States.

By PreventionGenetics PreventionGenetics

This panel specifically test the F10 gene.

More info about this panel

Bleeding Disorders Sequencing Panel with CNV Detection Panel

United States.

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 panel

Coagulation Factor Deficiency Sequencing Panel with CNV Detection Panel

United States.

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 panel

Factor 10 Deficiency Panel

India.

By GeneTech ATS GeneTech Private Limited

This panel specifically test the F10 gene.

More info about this panel

CentoICU platinum plus Panel

Germany.

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 panel

New Born testing (CentoICU) Panel

Germany.

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 panel

Factor X gene analysis Panel

United Kingdom.

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 panel

Factor X Deficiency Panel

Italy.

By Medical Genetics Laboratory Bambino Gesù Children's Hospital

This panel specifically test the F10 gene.

More info about this panel

Platelets, Coagulation disorders Panel Panel

Germany.

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 panel

aCGH Deletion/Duplication Analysis Panel

United States.

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 panel

Factor 10 deficiency Panel

Austria.

By Praxis fuer Humangenetik Wien

This panel specifically test the F10 gene.

More info about this panel

Factor X Deficiency Panel

United Kingdom.

By Regional Molecular Haemostasis Laboratory Birmingham Childrens Hospital NHS Foundation Trust

This panel specifically test the F10 gene.

More info about this panel

Factor 10 deficiency Panel

Slovakia.

By MedGene

This panel specifically test the F10 gene.

More info about this panel

F10 Panel

United States.

By Fulgent Genetics Fulgent Genetics

This panel specifically test the F10 gene.

More info about this panel

Bleeding Disorder/Coagulopathy Panel Panel

Finland.

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 panel

Coagulation Factor Deficiency Panel Panel

Finland.

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 panel

Comprehensive Hematology Panel Panel

Finland.

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 panel

AMYLOIDOSIS HEREDITARY NGS PANEL Panel

Spain.

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 panel

Bleeding Disorders , Panel Massive Sequencing (NGS) 23 Genes Panel

Spain.

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

More info about this panel


If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like ZSWIM9

Need help with a diagnosis?

Learn more about how to achieve it with Mendelian


Learn more