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.
Table of contents:
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.
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
Search interest in FPGT-TNNI3K
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