MYL4 gene related symptoms and diseases
All the information presented here about the MYL4 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 MYL4 gene
| Symptoms // Phenotype | % Cases |
|---|---|
| Paroxysmal atrial fibrillation | Very Common - Between 80% and 100% cases |
| Arrhythmia | Very Common - Between 80% and 100% cases |
| Permanent atrial fibrillation | Very Common - Between 80% and 100% cases |
| Atrial fibrillation | Very Common - Between 80% and 100% cases |
| Palpitations | Very Common - Between 80% and 100% cases |
Other less frequent symptoms and clinical features
Patients with MYL4 gene alterations may also develop some of the following symptoms and phenotypes:Not very common - Between 30% and 50% cases
- Pain
- Sinus bradycardia
- Bradycardia
- AV nodal tachycardia
- Abnormal electrophysiology of sinoatrial node origin
- Thromboembolic stroke
- ST segment elevation
- Abnormal atrioventricular conduction
And 12 more phenotypes, you can get all of them using our tools for rare diseases.
Rare diseases associated to MYL4 gene
Here you will find a list of rare diseases related to the MYL4. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
FAMILIAL ATRIAL FIBRILLATION
Alternate names
FAMILIAL ATRIAL FIBRILLATION Is also known as atrial fibrillation, autosomal dominant
Description
Familial atrial fibrillation is a rare, genetically heterogenous cardiac disease characterized by erratic activation of the atria with an irregular ventricular response, in various members of a single family. It may be asymptomatic or associated with palpitations, dyspnea and light-headedness. Concomitant rhythm disorders and cardiomyopathies are frequently reported.
Most common symptoms of FAMILIAL ATRIAL FIBRILLATION
- Pain
- Respiratory distress
- Arrhythmia
- Stroke
- Dilated cardiomyopathy
More info about FAMILIAL ATRIAL FIBRILLATION
ATRIAL FIBRILLATION, FAMILIAL, 18; ATFB18
Most common symptoms of ATRIAL FIBRILLATION, FAMILIAL, 18; ATFB18
- Arrhythmia
- Atrial fibrillation
- Palpitations
- Bradycardia
- Sinus bradycardia
More info about ATRIAL FIBRILLATION, FAMILIAL, 18; ATFB18
SOURCES: OMIM
Search interest in MYL4
Potential gene panels for MYL4 gene
Atrial Fibrillation Syndrome via MYL4 Gene Sequencing with CNV Detection Panel
United States.
By PreventionGenetics PreventionGenetics
This panel specifically test the MYL4 gene.
More info about this panel United States.
Comprehensive Cardiac Arrhythmia Sequencing Panel with CNV Detection Panel
United States.
By PreventionGenetics PreventionGenetics Comprehensive Cardiac Arrhythmia Sequencing Panel with CNV Detection that also includes the following genes: RYR2 SCN10A SCN1B SCN2B SCN4B SCN5A SNTA1 TGFB3 TNNI3 TRDN
More info about this panel United States.
Invitae Arrhythmia Comprehensive Panel Panel
United States.
By Invitae Invitae Arrhythmia Comprehensive Panel that also includes the following genes: RYR2 SCN5A TNNI3 TNNT2 TRDN TTN CACNA1C CACNB2 CALM1 CALM2
More info about this panel United States.
Invitae Arrhythmia and Cardiomyopathy Comprehensive Panel Panel
United States.
By Invitae Invitae Arrhythmia and Cardiomyopathy Comprehensive Panel that also includes the following genes: RYR2 SCN5A SGCD SLC22A5 TAZ TCAP TGFB3 TNNC1 TNNI3 TNNT2
More info about this panel United States.
MYL4 Panel
United States.
By Fulgent Genetics Fulgent Genetics
This panel specifically test the MYL4 gene.
More info about this panel United States.
Cardiomyopathy Panel Panel
Finland.
By Blueprint Genetics Cardiomyopathy Panel that also includes the following genes: RIT1 RRAS RYR2 SCN5A SCNN1B SCNN1G SCO2 SDHA SGCA SGCB
More info about this panel Finland.
Arrhythmia Panel Panel
Finland.
By Blueprint Genetics Arrhythmia Panel that also includes the following genes: RYR2 SCN10A SCN1B SCN5A TBX5 TGFB3 TNNI3 TNNT2 TRDN TTN
More info about this panel Finland.
Comprehensive Cardiology Panel Panel
Finland.
By Blueprint Genetics Comprehensive Cardiology Panel that also includes the following genes: RIT1 RRAS RYR2 SCN10A SCN1B SCN5A SCNN1B SCNN1G SCO2 SDHA
More info about this panel Finland.
Dilated Cardiomyopathy (DCM) Panel Panel
Finland.
By Blueprint Genetics Dilated Cardiomyopathy (DCM) Panel that also includes the following genes: SCN5A TAZ TBX20 TBX5 TCAP TNNC1 TNNI3 TNNT2 TPM1 TTN
More info about this panel Finland.
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