RASGRP2 gene related symptoms and diseases
All the information presented here about the RASGRP2 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: OMIM,NCBIGENE,HGNC,ORPHANET, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to RASGRP2 gene
| Symptoms // Phenotype | % Cases |
|---|---|
| Epistaxis | Very Common - Between 80% and 100% cases |
| Menorrhagia | Very Common - Between 80% and 100% cases |
| Prolonged bleeding time | Very Common - Between 80% and 100% cases |
| Impaired platelet aggregation | Very Common - Between 80% and 100% cases |
Rare diseases associated to RASGRP2 gene
Here you will find a list of rare diseases related to the RASGRP2. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
BLEEDING DISORDER DUE TO CALDAG-GEFI DEFICIENCY
Alternate names
BLEEDING DISORDER DUE TO CALDAG-GEFI DEFICIENCY Is also known as bleeding disorder due to calcium- and dag-regulated guanine exchange factor-1 deficiency
Description
Bleeding disorder due to CalDAG-GEFI deficiency is a rare hematologic disease due to defective platelet function and characterized by mucocutaneous bleeding starting in infancy (around 18 months of age), presenting with prolonged and severe epistaxis, hematomas and bleeding after tooth extraction. Massive menorrhagia and chronic anemia have also been reported.
Most common symptoms of BLEEDING DISORDER DUE TO CALDAG-GEFI DEFICIENCY
- Epistaxis
- Menorrhagia
- Prolonged bleeding time
- Impaired platelet aggregation
More info about BLEEDING DISORDER DUE TO CALDAG-GEFI DEFICIENCY
Search interest in RASGRP2
Potential gene panels for RASGRP2 gene
Skeletal Disorders and Joint Problems Sequencing Panel with CNV Detection Panel
United States.
By PreventionGenetics PreventionGenetics Skeletal Disorders and Joint Problems Sequencing Panel with CNV Detection that also includes the following genes: RMRP ROR2 RUNX2 SALL1 BMP1 BMP2 BMPR1B SF3B4 SH3BP2 FBXW4
More info about this panel United States.
Platelet bleeding disorders NGS panel Panel
United States.
By Connective Tissue Gene Tests Platelet bleeding disorders NGS panel that also includes the following genes: SMPD1 TBXA2R TBXAS1 VWF WAS WIPF1 GP6 HPS3 HPS4 ACTN1
More info about this panel United States.
Platelet bleeding disorders Deletion / Duplication panel Panel
United States.
By Connective Tissue Gene Tests Platelet bleeding disorders Deletion / Duplication panel that also includes the following genes: SMPD1 TBXA2R TBXAS1 VWF WAS WIPF1 GP6 HPS3 HPS4 ACTN1
More info about this panel United States.
Platelet bleeding disorders Comprehensive panel Panel
United States.
By Connective Tissue Gene Tests Platelet bleeding disorders Comprehensive panel that also includes the following genes: SMPD1 TBXA2R TBXAS1 VWF WAS WIPF1 GP6 HPS3 HPS4 ACTN1
More info about this panel United States.
Skeletal Dysplasia With Increased Bone Density: Sequencing Panel Panel
United States.
By EGL Genetic Diagnostics Eurofins Clinical Diagnostics Skeletal Dysplasia With Increased Bone Density: Sequencing Panel that also includes the following genes: TBXAS1 TCIRG1 TGFB1 TNFRSF11A TNFRSF11B TNFSF11 TYROBP CA2 SOST ANKH
More info about this panel United States.
Skeletal Dysplasia: Sequencing Panel Panel
United States.
By EGL Genetic Diagnostics Eurofins Clinical Diagnostics Skeletal Dysplasia: Sequencing Panel that also includes the following genes: ROR2 RUNX2 SALL1 BMP2 BMPR1B FBXW4 SHH SHOX SLC25A12 SLC26A2
More info about this panel United States.
Skeletal Dysplasias NGS panel Panel
United States.
By Fulgent Genetics Fulgent Genetics Skeletal Dysplasias NGS panel that also includes the following genes: ROR2 RUNX2 SALL1 BMP2 BMPR1B FBXW4 SHH SLC25A12 SLC26A2 SMARCAL1
More info about this panel United States.
RASGRP2 Panel
United States.
By Fulgent Genetics Fulgent Genetics
This panel specifically test the RASGRP2 gene.
More info about this panel United States.
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