F11 gene related symptoms and diseases
All the information presented here about the F11 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: NCBIGENE,ORPHANET,OMIM,HGNC, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to F11 gene
Symptoms // Phenotype | % Cases |
---|---|
Bruising susceptibility | Very Common - Between 80% and 100% cases |
Hematuria | Very Common - Between 80% and 100% cases |
Abnormal bleeding | Very Common - Between 80% and 100% cases |
Gastrointestinal hemorrhage | Very Common - Between 80% and 100% cases |
Hepatitis | Very Common - Between 80% and 100% cases |
Other less frequent symptoms and clinical features
Patients with F11 gene alterations may also develop some of the following symptoms and phenotypes:Commonly - More than 50% cases
- Epistaxis
- Menorrhagia
- Abnormal joint morphology
- Prolonged partial thromboplastin time
- Joint hemorrhage
- Reduced factor XI activity
- Chronic active hepatitis
- Reduced factor VII activity
And 2 more phenotypes, you can get all of them using our tools for rare diseases.
Rare diseases associated to F11 gene
Here you will find a list of rare diseases related to the F11. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
CONGENITAL FACTOR XI DEFICIENCY
Alternate names
CONGENITAL FACTOR XI DEFICIENCY Is also known as f11 deficiency, plasma thromboplastin antecedent deficiency, hemophilia c, rosenthal syndrome, rosenthal factor deficiency, pta deficiency
Description
Congenital factor XI deficiency is an inherited bleeding disorder characterized by reduced levels and activity of factor XI (FXI) resulting in moderate bleeding symptoms, usually occurring after trauma or surgery.
Most common symptoms of CONGENITAL FACTOR XI DEFICIENCY
- Bruising susceptibility
- Hematuria
- Abnormal bleeding
- Gastrointestinal hemorrhage
- Hepatitis
More info about CONGENITAL FACTOR XI DEFICIENCY
Search interest in F11
Potential gene panels for F11 gene
Hereditary factor XI deficiency disease Panel
By Center for Human Genetics, Inc
This panel specifically test the F11 gene.
More info about this panelAshkenazi Jewish Carrier Screening Panel Panel
By Center for Human Genetics, Inc Ashkenazi Jewish Carrier Screening Panel that also includes the following genes: BLM SMPD1 CLRN1 MCOLN1 PCDH15 TMEM216 DLD F11 FANCC FKTN
More info about this panelF11 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 F11 gene.
More info about this panelF11 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 F11 gene.
More info about this panelFactor XI Deficiency Panel
By Sheffield Diagnostic Genetics Service Sheffield Children's NHS Foundation Trust
This panel specifically test the F11 gene.
More info about this panelFactor XI deficiency (sequence analysis of F11 gene) Panel
By CGC Genetics
This panel specifically test the F11 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 panelHemophilia C via F11 Gene Sequencing with CNV Detection Panel
By PreventionGenetics PreventionGenetics
This panel specifically test the F11 gene.
More info about this panelFactor XI deficiency Panel
By Centogene AG - the Rare Disease Company
This panel specifically test the F11 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 panelF11 gene analysis Panel
By Molecular Haemostasis & Thrombosis GSTS Pathology - Guy's and St. Thomas' NHS Foundation Trust
This panel specifically test the F11 gene.
More info about this panelFactor XI Deficiency Panel
By Medical Genetics Laboratory Bambino Gesù Children's Hospital
This panel specifically test the F11 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 panelAshkenazi Jewish diseases Panel
By Asper Biogene Asper Biogene LLC Ashkenazi Jewish diseases that also includes the following genes: BLM BRCA1 BRCA2 SMN1 SMPD1 CLRN1 MCOLN1 PCDH15 LRRK2 CFTR
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 11 deficiency Panel
By Praxis fuer Humangenetik Wien
This panel specifically test the F11 gene.
More info about this panelFactor 11 Deficiency Panel
By Regional Molecular Haemostasis Laboratory Birmingham Childrens Hospital NHS Foundation Trust
This panel specifically test the F11 gene.
More info about this panelFamily Prep Screen Panel
By Counsyl Family Prep Screen that also includes the following genes: RMRP BCS1L RS1 SACS BLM SGCA SGCB SLC12A6 SLC17A5 SLC22A5
More info about this panelqCarrier Plus Panel
By Quantitative Genomic Medicine Laboratories, SL qCarrier Plus that also includes the following genes: RMRP RP2 RPE65 RPGR RPS6KA3 RS1 SACS SGCA SGCB SGSH
More info about this panelFactor 11 deficiency Panel
By MedGene
This panel specifically test the F11 gene.
More info about this panelPan-Ethnic Carrier Screen: Gene Sequencing Panel Panel
By EGL Genetic Diagnostics Eurofins Clinical Diagnostics Pan-Ethnic Carrier Screen: Gene Sequencing Panel that also includes the following genes: RMRP BCS1L RS1 SACS BLM SGCA SGCB SGCG SGSH SLC12A6
More info about this panelF11 Panel
By Fulgent Genetics Fulgent Genetics
This panel specifically test the F11 gene.
More info about this panelFactor XI Mutation Analysis (Ashkenazi Jewish) Panel
By Quest Diagnostics Nichols Institute San Juan Capistrano
This panel specifically test the F11 gene.
More info about this panelFactor XI Mutation Analysis (Ashkenazi Jewish) (NY) Panel
By Quest Diagnostics Nichols Institute San Juan Capistrano
This panel specifically test the F11 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 panelFACTOR XI DEFICIENCY Panel
By Laboratorio de Genetica Clinica SL
This panel specifically test the F11 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
More info about this panelplanTrue Extended Panel
By True Health Diagnostics planTrue Extended that also includes the following genes: RMRP RS1 BLM SLC17A5 SLC22A5 SLC26A2 SMN1 SMPD1 BTD TNNT1
More info about this panelPan-Ethnic Carrier Screen: Full Gene Sequencing and SMA Analysis Panel
By CEN4GEN Institute for Genomics and Molecular Diagnostics Pan-Ethnic Carrier Screen: Full Gene Sequencing and SMA Analysis that also includes the following genes: RMRP BCS1L SACS BLM SGCA SGCB SGCG SGSH SLC12A6 SLC17A5
More info about this panelIf you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like CFTR EHHADH ELP1 CHCHD2 RERE MYH11