TECRL gene related symptoms and diseases
All the information presented here about the TECRL gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: NCBIGENE,HGNC,OMIM,ORPHANET, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to TECRL gene
| Symptoms // Phenotype | % Cases |
|---|---|
| Myocardial infarction | Very Common - Between 80% and 100% cases |
| Arrhythmia | Very Common - Between 80% and 100% cases |
| Interstitial pulmonary abnormality | Uncommon - Between 30% and 50% cases |
| Allergy | Uncommon - Between 30% and 50% cases |
| Myocarditis | Uncommon - Between 30% and 50% cases |
Other less frequent symptoms and clinical features
Patients with TECRL gene alterations may also develop some of the following symptoms and phenotypes:Not very common - Between 30% and 50% cases
- Tubulointerstitial nephritis
- Aortic root aneurysm
- Acute kidney injury
- Pericarditis
- Abnormal heart valve morphology
- Elevated erythrocyte sedimentation rate
- Leukocytosis
- Coronary artery atherosclerosis
And 78 more phenotypes, you can get all of them using our tools for rare diseases.
Rare diseases associated to TECRL gene
Here you will find a list of rare diseases related to the TECRL. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
CATECHOLAMINERGIC POLYMORPHIC VENTRICULAR TACHYCARDIA
Alternate names
CATECHOLAMINERGIC POLYMORPHIC VENTRICULAR TACHYCARDIA Is also known as vtsip, cpvt, ventricular tachycardia, stress-induced polymorphic, malignant paroxysmal ventricular tachycardia, multifocal ventricular premature beats, double tachycardia induced by catecholamines, bidirectional tachycardia induced by catecholamine
Description
Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a severe genetic arrhythmogenic disorder characterized by adrenergically induced ventricular tachycardia (VT) manifesting as syncope and sudden death.
Most common symptoms of CATECHOLAMINERGIC POLYMORPHIC VENTRICULAR TACHYCARDIA
- Seizures
- Arrhythmia
- Vertigo
- Tachycardia
- Sudden cardiac death
More info about CATECHOLAMINERGIC POLYMORPHIC VENTRICULAR TACHYCARDIA
KAWASAKI DISEASE
Alternate names
KAWASAKI DISEASE Is also known as kd, infantile polyarteritis, mucocutaneous lymph node syndrome
Description
Kawasaki disease (KD) is a febrile, systemic, self-limiting vasculitis affecting children and characterized by inflammation in the medium sized vessels associated with coronary arterial aneurysms (CAA) that may be life threatening when untreated. KD is the most common cause of acquired heart disease in children in developed countries and is a risk factor for ischemic heart disease in adulthood.
Most common symptoms of KAWASAKI DISEASE
- Sensorineural hearing impairment
- Ptosis
- Fever
- Fatigue
- Edema
More info about KAWASAKI DISEASE
Search interest in TECRL
Potential gene panels for TECRL gene
Cardiac channelopathy Deletion/ Duplication panel Panel
United States.
By Connective Tissue Gene Tests Cardiac channelopathy Deletion/ Duplication panel that also includes the following genes: RYR2 SCN10A SCN1B SCN2B SCN4B SCN5A SEMA3A SNTA1 TRDN CACNA1C
More info about this panel United States.
Cardiac channelopathy Comprehensive panel Panel
United States.
By Connective Tissue Gene Tests Cardiac channelopathy Comprehensive panel that also includes the following genes: RYR2 SCN10A SCN1B SCN2B SCN4B SCN5A SEMA3A SNTA1 TRDN CACNA1C
More info about this panel United States.
Cardiac channelopathy NGS panel Panel
United States.
By Connective Tissue Gene Tests Cardiac channelopathy NGS panel that also includes the following genes: RYR2 SCN10A SCN1B SCN2B SCN4B SCN5A SEMA3A SNTA1 TRDN CACNA1C
More info about this panel United States.
Catecholaminergic polymorphic ventricular tachycardia NGS panel Panel
United States.
By Connective Tissue Gene Tests Catecholaminergic polymorphic ventricular tachycardia NGS panel that also includes the following genes: RYR2 TRDN CALM1 CALM2 CALM3 CASQ2 TECRL ANK2 KCNJ2
More info about this panel United States.
Catecholaminergic polymorphic ventricular tachycardia Comprehensive panel Panel
United States.
By Connective Tissue Gene Tests Catecholaminergic polymorphic ventricular tachycardia Comprehensive panel that also includes the following genes: RYR2 TRDN CALM1 CALM2 CALM3 CASQ2 TECRL ANK2 KCNJ2
More info about this panel United States.
Catecholaminergic polymorphic ventricular tachycardia Deletion / Duplication panel Panel
United States.
By Connective Tissue Gene Tests Catecholaminergic polymorphic ventricular tachycardia Deletion / Duplication panel that also includes the following genes: RYR2 TRDN CALM1 CALM2 CALM3 CASQ2 TECRL ANK2 KCNJ2
More info about this panel United States.
TECRL Panel
United States.
By Fulgent Genetics Fulgent Genetics
This panel specifically test the TECRL gene.
More info about this panel United States.
Long QT Syndrome (LQTS) Panel Panel
Finland.
By Blueprint Genetics Long QT Syndrome (LQTS) Panel that also includes the following genes: SCN5A CACNA1C CALM1 CALM2 CALM3 CAV3 NOS1AP TECRL AKAP9 ANK2
More info about this panel Finland.
Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT) Panel Panel
Finland.
By Blueprint Genetics Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT) Panel that also includes the following genes: RYR2 TRDN CALM1 CALM2 CALM3 CASQ2 TECRL ANK2 KCNJ2
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.
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