CTNNA3 gene related symptoms and diseases
All the information presented here about the CTNNA3 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: NCBIGENE,ORPHANET,OMIM,HGNC, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to CTNNA3 gene
Symptoms // Phenotype | % Cases |
---|---|
Cardiomyopathy | Rare - less than 30% cases |
Central apnea | Rare - less than 30% cases |
Premature birth | Rare - less than 30% cases |
Abnormal lung morphology | Rare - less than 30% cases |
Exercise intolerance | Rare - less than 30% cases |
Other less frequent symptoms and clinical features
Patients with CTNNA3 gene alterations may also develop some of the following symptoms and phenotypes:Rarely - Less than 30% cases
- Emphysema
- Wheezing
- Right ventricular hypertrophy
- Chronic lung disease
- Atelectasis
- Small for gestational age
- Right ventricular failure
- Diaphragmatic paralysis
And 27 more phenotypes, you can get all of them using our tools for rare diseases.
Rare diseases associated to CTNNA3 gene
Here you will find a list of rare diseases related to the CTNNA3. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 13; ARVD13
Alternate names
ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 13; ARVD13 Is also known as arvc13, arrhythmogenic right ventricular cardiomyopathy 13
Description
Arrhythmogenic right ventricular cardiomyopathy/dysplasia is characterized by progressive fibrofatty myocardial replacement, primarily of the right ventricle. The main clinical features are structural and functional abnormalities of the ventricles, electrocardiographic depolarization/repolarization changes, reentrant arrhythmias, and sudden death (summary by van Hengel et al., 2013).
Most common symptoms of ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 13; ARVD13
- Cardiomyopathy
- Congestive heart failure
- Arrhythmia
- Tachycardia
- Syncope
More info about ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 13; ARVD13
SOURCES: OMIM
BRONCHOPULMONARY DYSPLASIA
Alternate names
BRONCHOPULMONARY DYSPLASIA Is also known as bpd
Description
Bronchopulmonary dysplasia is a chronic respiratory disease that results from complications related to lung injury during the treatment of infant acute respiratory distress syndrome (see these terms) in low-birth-weight premature infants or from abnormal lung development in older infants. Clinical signs are tachypnea, tachycardia and signs of respiratory distress such as intercostal recession, grunting and nasal flaring.
Most common symptoms of BRONCHOPULMONARY DYSPLASIA
- Respiratory distress
- Dyspnea
- Cough
- Small for gestational age
- Sleep disturbance
More info about BRONCHOPULMONARY DYSPLASIA
FAMILIAL ISOLATED ARRHYTHMOGENIC VENTRICULAR DYSPLASIA, LEFT DOMINANT FORM
Alternate names
FAMILIAL ISOLATED ARRHYTHMOGENIC VENTRICULAR DYSPLASIA, LEFT DOMINANT FORM Is also known as familial isolated arrhythmogenic ventricular cardiomyopathy, left dominant form
More info about FAMILIAL ISOLATED ARRHYTHMOGENIC VENTRICULAR DYSPLASIA, LEFT DOMINANT FORM
SOURCES: ORPHANET
FAMILIAL ISOLATED ARRHYTHMOGENIC VENTRICULAR DYSPLASIA, BIVENTRICULAR FORM
Alternate names
FAMILIAL ISOLATED ARRHYTHMOGENIC VENTRICULAR DYSPLASIA, BIVENTRICULAR FORM Is also known as familial isolated arrhythmogenic ventricular cardiomyopathy, biventricular form
More info about FAMILIAL ISOLATED ARRHYTHMOGENIC VENTRICULAR DYSPLASIA, BIVENTRICULAR FORM
SOURCES: ORPHANET
FAMILIAL ISOLATED ARRHYTHMOGENIC VENTRICULAR DYSPLASIA, RIGHT DOMINANT FORM
Alternate names
FAMILIAL ISOLATED ARRHYTHMOGENIC VENTRICULAR DYSPLASIA, RIGHT DOMINANT FORM Is also known as familial isolated arrhythmogenic ventricular cardiomyopathy, right dominant form, familial isolated arrhythmogenic ventricular dysplasia, classic form, familial isolated arrhythmogenic ventricular cardiomyopathy, classic form
More info about FAMILIAL ISOLATED ARRHYTHMOGENIC VENTRICULAR DYSPLASIA, RIGHT DOMINANT FORM
SOURCES: ORPHANET
Search interest in CTNNA3
Potential gene panels for CTNNA3 gene
CTNNA3 Panel
By Institute for Human Genetics University Clinic Freiburg
This panel specifically test the CTNNA3 gene.
More info about this panelCardiomyopathy NGS Multi-Gene Panel (50 genes), Sequence & CNV analysis Panel
By Laboratory of genome diagnostics Academic Medical Center, University of Amsterdam Cardiomyopathy NGS Multi-Gene Panel (50 genes), Sequence & CNV analysis that also includes the following genes: SCN5A SGCD TAZ TCAP TNNC1 TNNI3 TNNT2 TPM1 TTN TTR
More info about this panelArrhythmogenic right ventricular dysplasia 13 (ARVD, sequence analysis of CTNNA3 gene) Panel
By CGC Genetics
This panel specifically test the CTNNA3 gene.
More info about this panelArrhythmogenic right ventricular dysplasia 13 (ARVD, sequence analysis of CTNNA3 gene) Panel
By CGC Genetics
This panel specifically test the CTNNA3 gene.
More info about this panelArrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy (ARVD/C) Panel Panel
By CeGaT GmbH Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy (ARVD/C) Panel that also includes the following genes: RYR2 TGFB3 TTN CTNNA3 DES TMEM43 DSC2 DSG2 DSP JUP
More info about this panelArrhythmogenic Right Ventricular Dysplasia/ Cardiomyopathy Panel
By Asper Biogene Asper Biogene LLC Arrhythmogenic Right Ventricular Dysplasia/ Cardiomyopathy that also includes the following genes: RYR2 TGFB3 TTN LDB3 CTNNA3 DES TMEM43 DSC2 DSG2 DSP
More info about this panelInherited Cardiovascular Diseases and Sudden Death Panel Panel
By Health in Code Inherited Cardiovascular Diseases and Sudden Death Panel that also includes the following genes: MRPL3 RYR2 SCN10A SCN1B SCN2B SCN4B SCN5A BMPR1B BMPR2 SGCA
More info about this panelVentricular Arrythmia & Sudden Death Panel with Structural Heart Disease Panel
By Health in Code Ventricular Arrythmia & Sudden Death Panel with Structural Heart Disease that also includes the following genes: MRPL3 RYR2 SCN10A SCN1B SCN2B SCN4B SCN5A SLC22A5 BRAF SLC25A4
More info about this panelVentricular Arrythmia & Sudden Death Panel without Structural Heart Disease Panel
By Health in Code Ventricular Arrythmia & Sudden Death Panel without Structural Heart Disease that also includes the following genes: RYR2 SCN10A SCN1B SCN2B SCN4B SCN5A SNTA1 TNNC1 TNNI3 TNNT2
More info about this panelCardiomyopathies Panel Panel
By Health in Code Cardiomyopathies Panel that also includes the following genes: MRPL3 RYR2 SCN5A SGCA SGCB SGCD SLC22A5 BRAF SLC25A4 SOS1
More info about this panelArrythmogenic Cardiomyopathy Panel Panel
By Health in Code Arrythmogenic Cardiomyopathy Panel that also includes the following genes: RYR2 SCN5A TGFB3 TTN CASQ2 LDB3 CTNNA3 DES TMEM43 DSC2
More info about this panelArrhythmogenic cardiomyopathy Panel
By Health in Code Arrhythmogenic cardiomyopathy that also includes the following genes: RYR2 SCN5A TGFB3 TTN CASQ2 LDB3 PERP PPP1R13L CTNNA3 CTNNB1
More info about this panelCardiovascular Diseases_General Panel Panel
By Health in Code Cardiovascular Diseases_General Panel that also includes the following genes: RIT1 MRPL3 RRAS RYR1 RYR2 SAR1B BLK SCN10A SCN1B SCN2B
More info about this panelArrhythmia General Panel Panel
By Health in Code Arrhythmia General Panel that also includes the following genes: RIT1 MRPL3 RRAS RYR2 SCN10A SCN1B SCN2B SCN4B SCN5A SCO2
More info about this panelCardiomyopathies General Panel Panel
By Health in Code Cardiomyopathies General Panel that also includes the following genes: RIT1 MRPL3 RRAS RYR2 SCN5A SCO2 SDHA SGCA SGCB SGCD
More info about this panelArrhythmias: Sequencing Panel Panel
By EGL Genetic Diagnostics Eurofins Clinical Diagnostics Arrhythmias: Sequencing Panel that also includes the following genes: RYR2 SCN1B SCN4B SCN5A SNTA1 TRDN CACNA1C CACNB2 CALM1 CASQ2
More info about this panelArrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy: Sequencing Panel Panel
By EGL Genetic Diagnostics Eurofins Clinical Diagnostics Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy: Sequencing Panel that also includes the following genes: RYR2 CTNNA3 TMEM43 DSC2 DSG2 DSP JUP PKP2
More info about this panelComprehensive Cardiovascular: Sequencing Panel Panel
By EGL Genetic Diagnostics Eurofins Clinical Diagnostics Comprehensive Cardiovascular: Sequencing Panel that also includes the following genes: RIT1 RYR2 SCN1B SCN4B SCN5A BMPR2 SGCD SKI SLC22A5 BRAF
More info about this panelCTNNA3 Panel
By Fulgent Genetics Fulgent Genetics
This panel specifically test the CTNNA3 gene.
More info about this panelCardiomyopathy Panel Panel
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 panelLeft Ventricular Non-Compaction Cardiomyopathy (LVNC) Panel Panel
By Blueprint Genetics Left Ventricular Non-Compaction Cardiomyopathy (LVNC) Panel that also includes the following genes: RYR2 SCN5A TCAP TNNT2 TPM1 TTN VCL JPH2 FBXO32 HCN4
More info about this panelArrhythmia Panel Panel
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 panelComprehensive Cardiology Panel Panel
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 panelArrhythmogenic Right Ventricular Cardiomyopathy (ARVC) Panel Panel
By Blueprint Genetics Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) Panel that also includes the following genes: RYR2 TGFB3 TTN LDB3 CDH2 CTNNA3 DES TMEM43 DSC2 DSG2
More info about this panelArrhythmogenic Right Ventricular Cardiomyopathy Panel Panel
By DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children Arrhythmogenic Right Ventricular Cardiomyopathy Panel that also includes the following genes: RYR2 TGFB3 CTNNA3 TMEM43 DSC2 DSG2 DSP JUP PKP2
More info about this panelCTNNA3 Gene Sequencing and Deletion/Duplication Analysis Panel
By DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
This panel specifically test the CTNNA3 gene.
More info about this panelFAMILIAL ISOLATED ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA: NGS PANEL Panel
By Laboratorio de Genetica Clinica SL FAMILIAL ISOLATED ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA: NGS PANEL that also includes the following genes: RYR2 TGFB3 CTNNA3 DES TMEM43 DSC2 DSG2 DSP JUP LMNA
More info about this panelVentricular Arrhythmia and Sudden Cardiac Death , Panel Massive Sequencing (NGS) 48 Genes Panel
By Reference Laboratory Genetics Ventricular Arrhythmia and Sudden Cardiac Death , Panel Massive Sequencing (NGS) 48 Genes that also includes the following genes: RYR2 SCN10A SCN1B SCN2B SCN4B SCN5A SNTA1 TGFB3 TNNC1 TNNI3
More info about this panelCardiology Genetic Panel (Full) , Panel Massive Sequencing (NGS) 96 Genes Panel
By Reference Laboratory Genetics Cardiology Genetic Panel (Full) , Panel Massive Sequencing (NGS) 96 Genes that also includes the following genes: RYR2 SCN1B SCN2B SCN4B SCN5A SGCD SLC25A3 SLC6A4 SNTA1 TAZ
More info about this panelTempus xO assay Panel
By Tempus Labs, Inc. Tempus xO assay that also includes the following genes: BCL6 RHEB RIPK1 RIPK2 RIPK3 RIT1 BCL7A BCL9 BCR ROBO2
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