FPGT-TNNI3K gene related symptoms and diseases

All the information presented here about the FPGT-TNNI3K gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: NCBIGENE,HGNC, Mendelian Rare Disease Search Engine.

Top 5 symptoms and clinical features associated to FPGT-TNNI3K gene

Symptoms // Phenotype % Cases
Cardiomyopathy Very Common - Between 80% and 100% cases
Supraventricular tachycardia Very Common - Between 80% and 100% cases
Multifocal atrial tachycardia Very Common - Between 80% and 100% cases
Left anterior fascicular block Very Common - Between 80% and 100% cases
Permanent atrial fibrillation Very Common - Between 80% and 100% cases

Other less frequent symptoms and clinical features

Patients with FPGT-TNNI3K gene alterations may also develop some of the following symptoms and phenotypes:
  • Commonly - More than 50% cases

  • Atrial arrhythmia
  • Paroxysmal atrial fibrillation
  • Atrial flutter
  • Reduced ejection fraction
  • Ventricular extrasystoles
  • Congestive heart failure
  • Right bundle branch block
  • Atrioventricular block

And 7 more phenotypes, you can get all of them using our tools for rare diseases.

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Rare diseases associated to FPGT-TNNI3K gene

Here you will find a list of rare diseases related to the FPGT-TNNI3K. You can also use our tool to get a more accurate diagnosis based on your current symptoms.


FAMILIAL ATRIAL TACHYARRHYTHMIA-INFRA-HISIAN CARDIAC CONDUCTION DISEASE


Most common symptoms of FAMILIAL ATRIAL TACHYARRHYTHMIA-INFRA-HISIAN CARDIAC CONDUCTION DISEASE

  • Cardiomyopathy
  • Congestive heart failure
  • Arrhythmia
  • Dyspnea
  • Dilated cardiomyopathy


More info about FAMILIAL ATRIAL TACHYARRHYTHMIA-INFRA-HISIAN CARDIAC CONDUCTION DISEASE

SOURCES: OMIM ORPHANET




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