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.

Mendelian

Accelerate your rare disease diagnosis with us

Learn more

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

SOURCES: ORPHANET OMIM

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

SOURCES: OMIM ORPHANET MESH


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

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

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

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

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

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

TECRL Panel

United States.

By Fulgent Genetics Fulgent Genetics

This panel specifically test the TECRL gene.

More info about this panel

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

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

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

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


If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like SBF2 SLC12A2

Need help with a diagnosis?

Learn more about how to achieve it with Mendelian


Learn more