NOS1AP gene related symptoms and diseases
All the information presented here about the NOS1AP gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: NCBIGENE,HGNC,ORPHANET,OMIM, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to NOS1AP gene
Symptoms // Phenotype | % Cases |
---|---|
Seizures | Very Common - Between 80% and 100% cases |
Arrhythmia | Very Common - Between 80% and 100% cases |
Sudden cardiac death | Very Common - Between 80% and 100% cases |
Syncope | Very Common - Between 80% and 100% cases |
Bradycardia | Very Common - Between 80% and 100% cases |
Other less frequent symptoms and clinical features
Patients with NOS1AP gene alterations may also develop some of the following symptoms and phenotypes:Commonly - More than 50% cases
- Cardiac arrest
- Ventricular tachycardia
- Ventricular arrhythmia
- Atrioventricular block
- Ventricular fibrillation
- Prolonged QT interval
- Epileptic spasms
- Torsade de pointes
And 3 more phenotypes, you can get all of them using our tools for rare diseases.
Rare diseases associated to NOS1AP gene
Here you will find a list of rare diseases related to the NOS1AP. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
ROMANO-WARD SYNDROME
Alternate names
ROMANO-WARD SYNDROME Is also known as romano-ward long qt syndrome
Description
Romano-Ward syndrome (RWS) is an autosomal dominant variant of the long QT syndrome (LQTS, see this term) characterized by syncopal episodes and electrocardiographic abnormalities (QT prolongation, T-wave abnormalities and torsade de pointes (TdP) ventricular tachycardia).
Most common symptoms of ROMANO-WARD SYNDROME
- Seizures
- Arrhythmia
- Sudden cardiac death
- Syncope
- Bradycardia
More info about ROMANO-WARD SYNDROME
Search interest in NOS1AP
Potential gene panels for NOS1AP gene
Autism Spectrum Disorders 53-Gene Panel Panel
By Center for Human Genetics, Inc Autism Spectrum Disorders 53-Gene Panel that also includes the following genes: RPL10 SYN1 SYNGAP1 TSPAN7 PCDH10 CNTNAP2 SH3KBP1 CACNA1H PCDH19 NLGN4X
More info about this panelNOS1AP Panel
By Institute for Human Genetics University Clinic Freiburg
This panel specifically test the NOS1AP gene.
More info about this panelCardiac channelopathy Deletion/ Duplication panel Panel
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 panelCardiac channelopathy Comprehensive panel Panel
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 panelCardiac channelopathy NGS panel Panel
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 panelLong QT syndrome Comprehensive panel Panel
By Connective Tissue Gene Tests Long QT syndrome Comprehensive panel that also includes the following genes: RYR2 SCN4B SCN5A SNTA1 TRDN CACNA1C CALM1 CALM2 CALM3 CAV3
More info about this panelLong QT syndrome NGS panel Panel
By Connective Tissue Gene Tests Long QT syndrome NGS panel that also includes the following genes: RYR2 SCN4B SCN5A SNTA1 TRDN CACNA1C CALM1 CALM2 CALM3 CAV3
More info about this panelLong QT syndrome Deletion / Duplication panel Panel
By Connective Tissue Gene Tests Long QT syndrome Deletion / Duplication panel that also includes the following genes: RYR2 SCN4B SCN5A SNTA1 TRDN CACNA1C CALM1 CALM2 CALM3 CAV3
More info about this panelLong QT Syndrome Extended Panel Panel
By Health in Code Long QT Syndrome Extended Panel that also includes the following genes: RYR2 SCN1B SCN4B SCN5A SNTA1 TRDN CACNA1C CALM1 CALM2 CALM3
More info about this panelVentricular arrhythmia and sudden death without structural heart disease Panel
By Health in Code Ventricular arrhythmia and sudden death without structural heart disease that also includes the following genes: RYR2 SCN10A SCN1B SCN2B SCN4B SCN5A SNTA1 TBX5 TNNC1 TNNI3
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 panelLONG QT SYNDROME Panel
By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases LONG QT SYNDROME that also includes the following genes: RYR2 SCN1B SCN4B SCN5A SNTA1 TRDN CACNA1C CALM1 CAV3 NOS1AP
More info about this panelFamilial Arrhythmia Full Gene Sequencing Panel Panel
By Integrated Genetics Westborough Integrated Genetics Familial Arrhythmia Full Gene Sequencing Panel that also includes the following genes: RYR2 SCN1B SCN4B SCN5A SNTA1 TGFB3 CACNA1C CACNB2 CASQ2 CAV3
More info about this panelNOS1AP Panel
By Fulgent Genetics Fulgent Genetics
This panel specifically test the NOS1AP gene.
More info about this panelLong QT Syndrome (LQTS) Panel Panel
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 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 panelAmiodarone response Panel
By Xcode Life Xcode Life Amiodarone response that also includes the following genes: NOS1AP CYP3A4
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