SCNN1G gene related symptoms and diseases
All the information presented here about the SCNN1G gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: NCBIGENE,OMIM,HGNC,ORPHANET, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to SCNN1G gene
| Symptoms // Phenotype | % Cases |
|---|---|
| Failure to thrive | Rare - less than 30% cases |
| Muscle weakness | Rare - less than 30% cases |
| Bronchiectasis | Rare - less than 30% cases |
| Hypokalemic metabolic alkalosis | Rare - less than 30% cases |
| Decreased circulating renin level | Rare - less than 30% cases |
Other less frequent symptoms and clinical features
Patients with SCNN1G gene alterations may also develop some of the following symptoms and phenotypes:Rarely - Less than 30% cases
- Metabolic alkalosis
- Cerebral ischemia
- Alkalosis
- Hypokalemia
- Nephropathy
- Constipation
- Arrhythmia
- Renal insufficiency
And 19 more phenotypes, you can get all of them using our tools for rare diseases.
Rare diseases associated to SCNN1G gene
Here you will find a list of rare diseases related to the SCNN1G. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
GENERALIZED PSEUDOHYPOALDOSTERONISM TYPE 1
Alternate names
GENERALIZED PSEUDOHYPOALDOSTERONISM TYPE 1 Is also known as pha i, autosomal recessive, autosomal recessive pseudohypoaldosteronism type 1
Description
Generalized pseudohypoaldosteronism type 1 (generalized PHA1) is a severe form of primary mineralocorticoid resistance with systemic involvement and salt loss in multiple organs.
Most common symptoms of GENERALIZED PSEUDOHYPOALDOSTERONISM TYPE 1
- Failure to thrive
- Vomiting
- Diarrhea
- Recurrent respiratory infections
- Acidosis
More info about GENERALIZED PSEUDOHYPOALDOSTERONISM TYPE 1
LIDDLE SYNDROME
Alternate names
LIDDLE SYNDROME Is also known as pseudohyperaldosteronism type 1, pseudoaldosteronism
Description
Liddle syndrome is a rare inherited form of hypertension characterized by severe early-onset hypertension associated with decreased plasmatic levels of potassium, renin and aldosterone.
Most common symptoms of LIDDLE SYNDROME
- Muscle weakness
- Hypertension
- Fatigue
- Renal insufficiency
- Arrhythmia
More info about LIDDLE SYNDROME
BRONCHIECTASIS WITH OR WITHOUT ELEVATED SWEAT CHLORIDE 3; BESC3
Alternate names
BRONCHIECTASIS WITH OR WITHOUT ELEVATED SWEAT CHLORIDE 3; BESC3 Is also known as cystic fibrosis-like syndrome
Most common symptoms of BRONCHIECTASIS WITH OR WITHOUT ELEVATED SWEAT CHLORIDE 3; BESC3
- Bronchiectasis
- Chronic bronchitis
More info about BRONCHIECTASIS WITH OR WITHOUT ELEVATED SWEAT CHLORIDE 3; BESC3
IDIOPATHIC BRONCHIECTASIS
Description
Idiopathic bronchiectasis (IB) is a progressive lung disease characterized by chronic dilation of the bronchi and destruction of the bronchial walls in the absence of any underlying cause (such as post infectious disease, aspiration, immunodeficiency, congenital abnormalities and ciliary anomalies).
More info about IDIOPATHIC BRONCHIECTASIS
SOURCES: ORPHANET
Search interest in SCNN1G
Potential gene panels for SCNN1G gene
Pseudohypoaldosteronism Type 1 Evaluation (SCNN1A, SCNN1B, SCNN1G) Panel
United States.
By Athena Diagnostics Inc Pseudohypoaldosteronism Type 1 Evaluation (SCNN1A, SCNN1B, SCNN1G) that also includes the following genes: SCNN1A SCNN1B SCNN1G
More info about this panel United States.
SCNN1G DNA Sequencing Test Panel
United States.
By Athena Diagnostics Inc
This panel specifically test the SCNN1G gene.
More info about this panel United States.
Monogenic Hypertension Evaluation Panel
United States.
By Athena Diagnostics Inc Monogenic Hypertension Evaluation that also includes the following genes: SCNN1B SCNN1G CYP11B1 HSD11B2
More info about this panel United States.
Liddle's Syndrome Evaluation Panel
United States.
By Athena Diagnostics Inc Liddle's Syndrome Evaluation that also includes the following genes: SCNN1B SCNN1G
More info about this panel United States.
Comprehensive Pulmonary Panel Panel
United States.
By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center Comprehensive Pulmonary Panel that also includes the following genes: RPGR SCNN1A SCNN1B SCNN1G BMPR1B BMPR2 SFTPA1 SFTPA2 SFTPB SFTPC
More info about this panel United States.
Primary Ciliary Dyskinesia and Cystic Fibrosis Panel Panel
United States.
By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center Primary Ciliary Dyskinesia and Cystic Fibrosis Panel that also includes the following genes: RPGR SCNN1A SCNN1B SCNN1G SPAG1 RSPH1 CFAP298 NME8 LRRC6 INVS
More info about this panel United States.
Cystic Fibrosis and CF-Related Disorders NGS Panel Panel
United States.
By Johns Hopkins DNA Diagnostic Laboratory Johns Hopkins Hospital Cystic Fibrosis and CF-Related Disorders NGS Panel that also includes the following genes: SCNN1A SCNN1B SCNN1G CA12 CFTR
More info about this panel United States.
Cystic Fibrosis Related Disorders NGS Panel Panel
United States.
By Johns Hopkins DNA Diagnostic Laboratory Johns Hopkins Hospital Cystic Fibrosis Related Disorders NGS Panel that also includes the following genes: SCNN1A SCNN1B SCNN1G CA12
More info about this panel United States.
Pseudohypoaldosteronism Type 1 NGS panel Panel
United States.
By Johns Hopkins DNA Diagnostic Laboratory Johns Hopkins Hospital Pseudohypoaldosteronism Type 1 NGS panel that also includes the following genes: SCNN1A SCNN1B SCNN1G NR3C2
More info about this panel United States.
Liddle Syndrome (pseudoprimary hyperaldosteronism) Panel
United States.
By Johns Hopkins DNA Diagnostic Laboratory Johns Hopkins Hospital Liddle Syndrome (pseudoprimary hyperaldosteronism) that also includes the following genes: SCNN1B SCNN1G
More info about this panel United States.
Liddle syndrome Panel
United States.
By Genetics Laboratory Shodair Children's Hospital
This panel specifically test the SCNN1G gene.
More info about this panel United States.
Bronchiectasis Panel (17 Genes) Panel
United States.
By Laboratory for Molecular Medicine Partners HealthCare Personalized Medicine Bronchiectasis Panel (17 Genes) that also includes the following genes: SCNN1A SCNN1B SCNN1G RSPH1 NME8 DNAI2 CFTR DNAAF2 RSPH9 RSPH4A
More info about this panel United States.
PulmoGene Panel (64 Genes) Panel
United States.
By Laboratory for Molecular Medicine Partners HealthCare Personalized Medicine PulmoGene Panel (64 Genes) that also includes the following genes: RPGR BDNF SCNN1A SCNN1B SCNN1G BMPR2 SFTPA1 SFTPA2 SFTPB SFTPC
More info about this panel United States.
SCNN1G. Complete sequencing Panel
Spain.
By Instituto de Medicina Genomica Instituto de Medicina Genomica
This panel specifically test the SCNN1G gene.
More info about this panel Spain.
SCNN1G. Complete sequencing Panel
Spain.
By Instituto de Medicina Genomica Instituto de Medicina Genomica
This panel specifically test the SCNN1G gene.
More info about this panel Spain.
Liddle syndrome (sequence analysis of SCNN1G gene) Panel
Portugal.
By CGC Genetics
This panel specifically test the SCNN1G gene.
More info about this panel Portugal.
Pseudohypoaldosteronism type I (sequence analysis of SCNN1G gene) Panel
Portugal.
By CGC Genetics
This panel specifically test the SCNN1G gene.
More info about this panel Portugal.
Pseudohypoaldosteronism (NGS panel of 9 genes) Panel
Portugal.
By CGC Genetics Pseudohypoaldosteronism (NGS panel of 9 genes) that also includes the following genes: SCNN1A SCNN1B SCNN1G WNK1 WNK4 CUL3 CYP11B2 KLHL3 NR3C2
More info about this panel Portugal.
Pseudohypoaldosteronism (NGS panel of 9 genes) Panel
Portugal.
By CGC Genetics Pseudohypoaldosteronism (NGS panel of 9 genes) that also includes the following genes: SCNN1A SCNN1B SCNN1G WNK1 WNK4 CUL3 CYP11B2 KLHL3 NR3C2
More info about this panel Portugal.
Pseudohypoaldosteronism type 1 autosomal recessive Panel
Germany.
By Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders Pseudohypoaldosteronism type 1 autosomal recessive that also includes the following genes: SCNN1A SCNN1B SCNN1G
More info about this panel Germany.
Bronchiectasis Panel
Germany.
By Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders Bronchiectasis that also includes the following genes: SCNN1A SCNN1B SCNN1G
More info about this panel Germany.
Bronchiectasis with or without elevated sweat chloride 3 Panel
Germany.
By Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders
This panel specifically test the SCNN1G gene.
More info about this panel Germany.
Liddle syndrome Panel
Germany.
By Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders Liddle syndrome that also includes the following genes: SCNN1B SCNN1G STK39 NEDD4 NEDD4L NR3C2 OXSR1
More info about this panel Germany.
Liddle Syndrome and Autosomal Recessive Pseudohypoaldosteronism Type 1 via SCNN1G Gene Sequencing with CNV Detection Panel
United States.
By PreventionGenetics PreventionGenetics
This panel specifically test the SCNN1G gene.
More info about this panel United States.
Pseudohypoaldosteronism Type I Sequencing Panel with CNV Detection Panel
United States.
By PreventionGenetics PreventionGenetics Pseudohypoaldosteronism Type I Sequencing Panel with CNV Detection that also includes the following genes: SCNN1A SCNN1B SCNN1G NR3C2
More info about this panel United States.
Liddle syndrome Panel
Germany.
By Institute of Human Genetics Uniklinik RWTH Aachen Liddle syndrome that also includes the following genes: SCNN1B SCNN1G
More info about this panel Germany.
Hypertension Panel
Germany.
By Institute of Human Genetics Uniklinik RWTH Aachen Hypertension that also includes the following genes: SCNN1A SCNN1G SDHA SDHB SDHC SDHD WNK1 WNK4 CUL3 CYP17A1
More info about this panel Germany.
Hereditary kidney disorders - different panels Panel
Germany.
By Institute of Human Genetics Uniklinik RWTH Aachen Hereditary kidney disorders - different panels that also includes the following genes: BCS1L ROBO2 CNNM2 CFB SALL1 ATXN10 SCNN1A SCNN1B SCNN1G SDCCAG8
More info about this panel Germany.
Bartter Syndrome panel Panel
Germany.
By Centogene AG - the Rare Disease Company Bartter Syndrome panel that also includes the following genes: SCNN1A SCNN1B SCNN1G SLC12A1 SLC12A2 SLC12A3 SLC12A7 SLC4A4 CA2 SLC12A5
More info about this panel Germany.
Pseudohypoaldosteronism, type I, autosomal recessive Panel
Germany.
By Centogene AG - the Rare Disease Company
This panel specifically test the SCNN1G gene.
More info about this panel Germany.
Liddle syndrome Panel
Germany.
By Centogene AG - the Rare Disease Company
This panel specifically test the SCNN1G gene.
More info about this panel Germany.
Comprehensive pulmonary disease panel Panel
Germany.
By Centogene AG - the Rare Disease Company Comprehensive pulmonary disease panel that also includes the following genes: BDNF SCNN1A SCNN1B SCNN1G BMPR2 SFTPA1 SFTPA2 SFTPB SFTPC SFTPD
More info about this panel Germany.
Pseudohypoaldosteronism Panel Panel
Germany.
By CeGaT GmbH Pseudohypoaldosteronism Panel that also includes the following genes: SCNN1A SCNN1B SCNN1G WNK1 WNK4 CUL3 HSD11B2 KLHL3 NR3C2
More info about this panel Germany.
Single gene testing SCNN1G Panel
Germany.
By CeGaT GmbH
This panel specifically test the SCNN1G gene.
More info about this panel Germany.
Pseudohypoaldosteronism type 1, autosomal reccesive: SCNN1G gene sequence analysis Panel
Spain.
By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
This panel specifically test the SCNN1G gene.
More info about this panel Spain.
Liddle syndrome: SCNN1G gene sequence analysis Panel
Spain.
By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
This panel specifically test the SCNN1G gene.
More info about this panel Spain.
BARTTER SYNDROME Panel
Spain.
By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases BARTTER SYNDROME that also includes the following genes: SCNN1A SCNN1B SCNN1G SLC12A1 SLC12A2 SLC12A3 SLC12A7 SLC4A4 CA2 SLC12A5
More info about this panel Spain.
Ciliopathies: Sequencing Panel Panel
United States.
By EGL Genetic Diagnostics Eurofins Clinical Diagnostics Ciliopathies: Sequencing Panel that also includes the following genes: RPE65 RPGR ATXN10 SCNN1A SCNN1B SCNN1G SDCCAG8 TSC1 TSC2 CEP41
More info about this panel United States.
Bronchiectasis: Sequencing Panel Panel
United States.
By EGL Genetic Diagnostics Eurofins Clinical Diagnostics Bronchiectasis: Sequencing Panel that also includes the following genes: SCNN1A SCNN1B SCNN1G NME8 DNAI2 CFTR DNAAF2 RSPH9 RSPH4A DNAL1
More info about this panel United States.
Pulmonary Disease: Comprehensive Sequencing Panel Panel
United States.
By EGL Genetic Diagnostics Eurofins Clinical Diagnostics Pulmonary Disease: Comprehensive Sequencing Panel that also includes the following genes: BDNF SCNN1A SCNN1B SCNN1G BMPR2 SFTPB SFTPC SFTPD STAT3 TERT
More info about this panel United States.
Bronchiectasis: Deletion/Duplication Panel Panel
United States.
By EGL Genetic Diagnostics Eurofins Clinical Diagnostics Bronchiectasis: Deletion/Duplication Panel that also includes the following genes: SCNN1A SCNN1B SCNN1G NME8 DNAI2 CFTR DNAAF2 RSPH9 RSPH4A DNAL1
More info about this panel United States.
Bronchiectasis NGS Panel Panel
United States.
By Fulgent Genetics Fulgent Genetics Bronchiectasis NGS Panel that also includes the following genes: SCNN1A SCNN1B SCNN1G NME8 DNAI2 CFTR DNAAF2 RSPH9 RSPH4A DNAL1
More info about this panel United States.
Lung Disorders NGS Panel Panel
United States.
By Fulgent Genetics Fulgent Genetics Lung Disorders NGS Panel that also includes the following genes: BDNF SCNN1A SCNN1B SCNN1G BMPR2 SFTPA1 SFTPA2 SFTPB SFTPC TERC
More info about this panel United States.
SCNN1G Panel
United States.
By Fulgent Genetics Fulgent Genetics
This panel specifically test the SCNN1G gene.
More info about this panel United States.
KidneySeq - 264 Genes Panel
United States.
By Iowa Institute of Human Genetics University of Iowa KidneySeq - 264 Genes that also includes the following genes: ROBO2 CNNM2 SALL1 ATXN10 SCNN1A SCNN1B SCNN1G SDCCAG8 BMP4 SEMA3E
More info about this panel United States.
Cardiomyopathy Panel Panel
Finland.
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 panel Finland.
Pseudohypoaldosteronism Panel Panel
Finland.
By Blueprint Genetics Pseudohypoaldosteronism Panel that also includes the following genes: SCNN1A SCNN1B SCNN1G WNK1 WNK4 CUL3 HSD11B2 KCNJ5 KLHL3 NR3C2
More info about this panel Finland.
Liddle Syndrome Panel Panel
Finland.
By Blueprint Genetics Liddle Syndrome Panel that also includes the following genes: SCNN1B SCNN1G
More info about this panel Finland.
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 Finland.
Liddle syndrome Panel
Spain.
By Bioarray
This panel specifically test the SCNN1G gene.
More info about this panel Spain.
Pseudohypoaldosteronism type 1, autosomal recessive Panel
Spain.
By Bioarray
This panel specifically test the SCNN1G gene.
More info about this panel Spain.
LIDDLE SYNDROME (PSEUDOALDOSTERONISM) Panel
Spain.
By Laboratorio de Genetica Clinica SL LIDDLE SYNDROME (PSEUDOALDOSTERONISM) that also includes the following genes: SCNN1B SCNN1G
More info about this panel Spain.
PSEUDOHYPOALDOSTERONISM, GENERALIZED, TYPE 1 (AUTOSOMAL RECESSIVE) Panel
Spain.
By Laboratorio de Genetica Clinica SL PSEUDOHYPOALDOSTERONISM, GENERALIZED, TYPE 1 (AUTOSOMAL RECESSIVE) that also includes the following genes: SCNN1A SCNN1B SCNN1G
More info about this panel Spain.
PSEUDOHYPERALDOSTERONISM TYPE 1 (LIDDLE SYNDROME) Panel
Spain.
By Laboratorio de Genetica Clinica SL PSEUDOHYPERALDOSTERONISM TYPE 1 (LIDDLE SYNDROME) that also includes the following genes: SCNN1B SCNN1G
More info about this panel Spain.
PSEUDOHYPOALDOSTERONISM NGS PANEL Panel
Spain.
By Laboratorio de Genetica Clinica SL PSEUDOHYPOALDOSTERONISM NGS PANEL that also includes the following genes: SCNN1A SCNN1B SCNN1G WNK1 WNK4 CUL3 HSD11B2 KLHL3 NR3C2
More info about this panel Spain.
BARTTER SYNDROME NGS PANEL Panel
Spain.
By Laboratorio de Genetica Clinica SL BARTTER SYNDROME NGS PANEL that also includes the following genes: SCNN1A SCNN1B SCNN1G SLC12A1 SLC12A2 SLC12A3 SLC12A7 SLC4A4 CA2 SLC12A5
More info about this panel Spain.
Autosomal Dominant Pseudohypoaldosteronism Type 1 , Sequencing SCNN1G Gene Panel
Spain.
By Reference Laboratory Genetics
This panel specifically test the SCNN1G gene.
More info about this panel Spain.
Liddle Disease, Sequencing SCNN1G Gene Panel
Spain.
By Reference Laboratory Genetics
This panel specifically test the SCNN1G gene.
More info about this panel Spain.
Autosomal Recessive Pseudohypoaldosteronism Type 1 , Sequencing SCNN1G Gene Panel
Spain.
By Reference Laboratory Genetics
This panel specifically test the SCNN1G gene.
More info about this panel Spain.
Bartter Syndrome and related disorders , Panel Massive Sequencing (NGS) 22 Genes Panel
Spain.
By Reference Laboratory Genetics Bartter Syndrome and related disorders , Panel Massive Sequencing (NGS) 22 Genes that also includes the following genes: SCNN1A SCNN1B SCNN1G SLC12A1 SLC12A3 CA2 WNK1 WNK4 CASR BSND
More info about this panel Spain.
Pseudohypoaldosteronism , Panel Massive Sequencing (NGS) 9 Genes Panel
Spain.
By Reference Laboratory Genetics Pseudohypoaldosteronism , Panel Massive Sequencing (NGS) 9 Genes that also includes the following genes: SCNN1A SCNN1B SCNN1G WNK1 WNK4 CUL3 HSD11B2 KLHL3 NR3C2
More info about this panel Spain.
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