SDCCAG8 gene related symptoms and diseases
All the information presented here about the SDCCAG8 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: OMIM,NCBIGENE,ORPHANET,HGNC, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to SDCCAG8 gene
Symptoms // Phenotype | % Cases |
---|---|
Intellectual disability | Common - Between 50% and 80% cases |
Hearing impairment | Common - Between 50% and 80% cases |
Retinal degeneration | Common - Between 50% and 80% cases |
Short stature | Common - Between 50% and 80% cases |
Hepatic fibrosis | Uncommon - Between 30% and 50% cases |
Other less frequent symptoms and clinical features
Patients with SDCCAG8 gene alterations may also develop some of the following symptoms and phenotypes:Not very common - Between 30% and 50% cases
- Nephronophthisis
- Renal dysplasia
- Renal cyst
- Rod-cone dystrophy
- Renal insufficiency
- Global developmental delay
- Stage 5 chronic kidney disease
- Nystagmus
And 77 more phenotypes, you can get all of them using our tools for rare diseases.
Rare diseases associated to SDCCAG8 gene
Here you will find a list of rare diseases related to the SDCCAG8. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
BARDET-BIEDL SYNDROME
Alternate names
BARDET-BIEDL SYNDROME Is also known as bbs
Description
Bardet-Biedl syndrome (BBS) is a ciliopathy with multisystem involvement.
Most common symptoms of BARDET-BIEDL SYNDROME
- Intellectual disability
- Short stature
- Hearing impairment
- Nystagmus
- Cryptorchidism
More info about BARDET-BIEDL SYNDROME
SOURCES: ORPHANET
SENIOR-LOKEN SYNDROME
Alternate names
SENIOR-LOKEN SYNDROME Is also known as renal-retinal syndrome, juvenile nephronophthisis with leber amaurosis, loken-senior syndrome, renal dysplasia-retinal aplasia syndrome, nephronophthisis with retinal dystrophy, slsn, renal dysplasia and retinal aplasia, senior-loken syndrome
Description
Senior-Loken syndrome (SLSN) is a very rare autosomal recessive oculo-renal disease characterized by the association of nephronophthisis (NPHP), a chronic kidney disease, with retinal dystrophy.
Most common symptoms of SENIOR-LOKEN SYNDROME
- Intellectual disability
- Global developmental delay
- Short stature
- Hearing impairment
- Ataxia
More info about SENIOR-LOKEN SYNDROME
SENIOR-LOKEN SYNDROME 7; SLSN7
Most common symptoms of SENIOR-LOKEN SYNDROME 7; SLSN7
- Retinal degeneration
- Nephronophthisis
More info about SENIOR-LOKEN SYNDROME 7; SLSN7
SOURCES: OMIM
BARDET-BIEDL SYNDROME 16; BBS16
Description
BBS16 is an autosomal recessive ciliopathy characterized by retinal degeneration, obesity, renal disease, and cognitive impairment. Although polydactyly is considered a primary feature of BBS overall, it has not been reported in any BBS16 patient (Billingsley et al., 2012).For a general phenotypic description and a discussion of genetic heterogeneity of Bardet-Biedl syndrome, see BBS1 (OMIM ).
Most common symptoms of BARDET-BIEDL SYNDROME 16; BBS16
- Intellectual disability
- Global developmental delay
- Short stature
- Hearing impairment
- Cognitive impairment
More info about BARDET-BIEDL SYNDROME 16; BBS16
SOURCES: OMIM
Search interest in SDCCAG8
Potential gene panels for SDCCAG8 gene
Bardet-Biedl Syndrome Panel Panel
By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center Bardet-Biedl Syndrome Panel that also includes the following genes: SDCCAG8 ARL6 TRIM32 IFT27 BBS7 TTC8 INPP5E ADIPOR1 BBS10 BBS12
More info about this panelCiliopathies Panel
By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University Ciliopathies that also includes the following genes: RPE65 RPGR SDCCAG8 TSC1 TSC2 CEP41 TULP1 USH1C USH2A CLRN1
More info about this panelBardet-Biedl Syndrome Sequencing Panel Panel
By Genetic Services Laboratory University of Chicago Bardet-Biedl Syndrome Sequencing Panel that also includes the following genes: SDCCAG8 ARL6 TRIM32 BBS7 TTC8 IFT74 BBS10 BBS12 WDPCP CEP290
More info about this panelMonogenic Obesity Sequencing Panel Panel
By Genetic Services Laboratory University of Chicago Monogenic Obesity Sequencing Panel that also includes the following genes: SDCCAG8 SIM1 UCP3 ARL6 TRIM32 AFF4 PHF6 SETD2 BBS7 TTC8
More info about this panelNephronophthisis Deletion/Duplication Panel Panel
By Genetic Services Laboratory University of Chicago Nephronophthisis Deletion/Duplication Panel that also includes the following genes: SDCCAG8 NEK8 ZNF423 INVS CEP83 DCDC2 WDR19 NPHP4 TTC21B ANKS6
More info about this panelRenal Cystic Disorders Sequencing Panel Panel
By Genetic Services Laboratory University of Chicago Renal Cystic Disorders Sequencing Panel that also includes the following genes: SALL1 SDCCAG8 HNF1B TFAP2A TSC1 TSC2 CEP41 UMOD VHL ARL6
More info about this panelNephronophthisis Sequencing Panel Panel
By Genetic Services Laboratory University of Chicago Nephronophthisis Sequencing Panel that also includes the following genes: SDCCAG8 NEK8 ZNF423 INVS CEP83 DCDC2 WDR19 NPHP4 TTC21B ANKS6
More info about this panelBardet-Biedl Syndrome Deletion/Duplication Panel Panel
By Genetic Services Laboratory University of Chicago Bardet-Biedl Syndrome Deletion/Duplication Panel that also includes the following genes: SDCCAG8 ARL6 TRIM32 BBS7 TTC8 IFT74 BBS10 BBS12 WDPCP CEP290
More info about this panelMonogenic Obesity Deletion/Duplication Panel Panel
By Genetic Services Laboratory University of Chicago Monogenic Obesity Deletion/Duplication Panel that also includes the following genes: SDCCAG8 SIM1 UCP3 ARL6 TRIM32 AFF4 PHF6 SETD2 BBS7 TTC8
More info about this panelSenior-Loken syndrome 7 (sequence analysis of SDCCAG8 gene) Panel
By CGC Genetics
This panel specifically test the SDCCAG8 gene.
More info about this panelBardet-Biedl syndrome (NGS panel for 22 genes) Panel
By CGC Genetics Bardet-Biedl syndrome (NGS panel for 22 genes) that also includes the following genes: SDCCAG8 ARL6 TRIM32 IFT27 BBS7 TTC8 BBS10 BBS12 WDPCP BBIP1
More info about this panelNephronophthisis (NGS panel for 19 genes) Panel
By CGC Genetics Nephronophthisis (NGS panel for 19 genes) that also includes the following genes: SDCCAG8 NEK8 ZNF423 INVS CEP83 DCDC2 WDR19 NPHP4 TTC21B ANKS6
More info about this panelCiliopathies (NGS panel for 90 genes) Panel
By CGC Genetics Ciliopathies (NGS panel for 90 genes) that also includes the following genes: SDCCAG8 SPAG1 CEP41 RSPH1 CFAP298 ARL6 NEK8 TMEM237 TRIM32 NME8
More info about this panelNephronophthisis and Senior-Loken Syndrome Sequencing Panel with CNV Detection Panel
By PreventionGenetics PreventionGenetics Nephronophthisis and Senior-Loken Syndrome Sequencing Panel with CNV Detection that also includes the following genes: SDCCAG8 NEK8 ZNF423 INVS CEP83 DCDC2 WDR19 NPHP4 TTC21B ANKS6
More info about this panelNephronophthisis / Senior-Loken Syndrome and Bardet-Biedl Syndrome via SDCCAG8 Gene Sequencing with CNV Detection Panel
By PreventionGenetics PreventionGenetics
This panel specifically test the SDCCAG8 gene.
More info about this panelBardet-Biedl Syndrome Sequencing Panel with CNV Detection Panel
By PreventionGenetics PreventionGenetics Bardet-Biedl Syndrome Sequencing Panel with CNV Detection that also includes the following genes: SDCCAG8 ARL6 TRIM32 IFT27 BBS7 TTC8 IFT74 BBS10 BBS12 C8orf37
More info about this panelComprehensive Inherited Retinal Dystrophies (includes RPGR ORF15) Sequencing Panel with CNV Detection Panel
By PreventionGenetics PreventionGenetics Comprehensive Inherited Retinal Dystrophies (includes RPGR ORF15) Sequencing Panel with CNV Detection that also includes the following genes: RGS9 RHO GRK1 RLBP1 ROM1 RP1 RP2 RP9 RPE65 RPGR
More info about this panelCiliopathy Sequencing Panel with CNV Detection Panel
By PreventionGenetics PreventionGenetics Ciliopathy Sequencing Panel with CNV Detection that also includes the following genes: RPGR SDCCAG8 SPAG1 CEP41 RSPH1 ZIC3 CFAP298 ARL6 NEK8 TMEM237
More info about this panelHereditary Cystic Kidney Diseases Sequencing Panel with CNV Detection Panel
By PreventionGenetics PreventionGenetics Hereditary Cystic Kidney Diseases Sequencing Panel with CNV Detection that also includes the following genes: SDCCAG8 HNF1B TSC1 TSC2 UMOD VHL NEK8 DNAJB11 ZNF423 DICER1
More info about this panelComprehensive Monogenic Obesity Panel with CNV Detection Panel
By PreventionGenetics PreventionGenetics Comprehensive Monogenic Obesity Panel with CNV Detection that also includes the following genes: BDNF SDCCAG8 SIM1 TUB UCP3 KDM6A ARL6 RAB23 TRIM32 PHF6
More info about this panelNephronophthisis and related disorders NGS panel Panel
By Connective Tissue Gene Tests Nephronophthisis and related disorders NGS panel that also includes the following genes: SDCCAG8 CEP41 NEK8 ZNF423 TRAF3IP1 INVS CEP83 DCDC2 WDR19 NPHP4
More info about this panelNephronophthisis and related disorders Comprehensive panel Panel
By Connective Tissue Gene Tests Nephronophthisis and related disorders Comprehensive panel that also includes the following genes: SDCCAG8 CEP41 NEK8 ZNF423 TRAF3IP1 INVS CEP83 DCDC2 WDR19 NPHP4
More info about this panelNephronophthisis and related disorders Deletion / Duplication panel Panel
By Connective Tissue Gene Tests Nephronophthisis and related disorders Deletion / Duplication panel that also includes the following genes: SDCCAG8 CEP41 NEK8 ZNF423 TRAF3IP1 INVS CEP83 DCDC2 WDR19 NPHP4
More info about this panelMental retardation - different panels Panel
By Institute of Human Genetics Uniklinik RWTH Aachen Mental retardation - different panels that also includes the following genes: RGS7 RIT1 RMRP BCS1L RPL10 RPS6KA3 RRAS SALL1 SC5D ATXN10
More info about this panelHereditary kidney disorders - different panels Panel
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 panelNephronophthisis panel Panel
By Centogene AG - the Rare Disease Company Nephronophthisis panel that also includes the following genes: SDCCAG8 NEK8 ZNF423 INVS NPHP4 ANKS6 IQCB1 CEP290 RPGRIP1L CEP164
More info about this panelSenior-Loken syndrome 7 Panel
By Centogene AG - the Rare Disease Company
This panel specifically test the SDCCAG8 gene.
More info about this panelBardet Biedl panel Panel
By Centogene AG - the Rare Disease Company Bardet Biedl panel that also includes the following genes: SDCCAG8 ARL6 TRIM32 BBS7 TTC8 BBS10 BBS12 WDPCP CCDC28B CEP290
More info about this panelAllNeuro panel Panel
By Centogene AG - the Rare Disease Company AllNeuro panel that also includes the following genes: BCS1L ROR2 RPL10 BDNF RPS6KA3 RTN2 RYR1 SACS BIN1 SBF1
More info about this panelBardet Biedl Syndrome Panel Panel
By CeGaT GmbH Bardet Biedl Syndrome Panel that also includes the following genes: SDCCAG8 ARL6 TRIM32 IFT27 BBS7 TTC8 TTC21B BBS10 BBS12 WDPCP
More info about this panelSenior Loken Syndrome Panel Panel
By CeGaT GmbH Senior Loken Syndrome Panel that also includes the following genes: SDCCAG8 IFT81 ZNF423 TRAF3IP1 INVS WDR19 NPHP4 IQCB1 CEP290 CEP164
More info about this panelBardet Biedl Syndrome Panel Panel
By CeGaT GmbH Bardet Biedl Syndrome Panel that also includes the following genes: SDCCAG8 ARL6 TRIM32 IFT27 BBS7 TTC8 TTC21B BBS10 BBS12 WDPCP
More info about this panelRenal Dysplasia, Renal Agenesia, CAKUT Panel Panel
By CeGaT GmbH Renal Dysplasia, Renal Agenesia, CAKUT Panel that also includes the following genes: ROBO2 SDCCAG8 BMP4 SIX1 SIX5 SPRY1 TBX18 HNF1B TFAP2A UPK3A
More info about this panelSenior Loken Syndrome Panel Panel
By CeGaT GmbH Senior Loken Syndrome Panel that also includes the following genes: SDCCAG8 IFT81 ZNF423 TRAF3IP1 INVS WDR19 NPHP4 IQCB1 CEP290 CEP164
More info about this panelSenior-Loken Syndrome Panel Panel
By CeGaT GmbH Senior-Loken Syndrome Panel that also includes the following genes: SDCCAG8 IFT81 ZNF423 TRAF3IP1 INVS WDR19 NPHP4 IQCB1 CEP290 CEP164
More info about this panelBardet-Biedl Syndrome Panel Panel
By CeGaT GmbH Bardet-Biedl Syndrome Panel that also includes the following genes: SDCCAG8 ARL6 TRIM32 IFT27 BBS7 TTC8 TTC21B BBS10 BBS12 WDPCP
More info about this panelBardet Biedl Syndrome Panel
By Asper Biogene Asper Biogene LLC Bardet Biedl Syndrome that also includes the following genes: SDCCAG8 ARL6 TRIM32 PHF6 BBS7 TTC8 BBS10 BBS12 WDPCP CCDC28B
More info about this panelEye diseases comprehensive panel Panel
By Asper Biogene Asper Biogene LLC Eye diseases comprehensive panel that also includes the following genes: RGS9 RHO GRK1 RLBP1 ROM1 RP1 RP2 RP9 RPE65 RPGR
More info about this panelSenior-Loken Syndrome Panel
By Asper Biogene Asper Biogene LLC Senior-Loken Syndrome that also includes the following genes: SDCCAG8 TRAF3IP1 INVS WDR19 NPHP4 IQCB1 CEP290 NPHP1 NPHP3
More info about this panelRetinal Dystrophy Panel Panel
By Molecular Vision Laboratory Retinal Dystrophy Panel that also includes the following genes: RGS9 RHO GRK1 RLBP1 ROM1 RP1 RP2 RP9 RPE65 RPGR
More info about this panelBardet-Biedl syndrome panel Panel
By Molecular Vision Laboratory Bardet-Biedl syndrome panel that also includes the following genes: SDCCAG8 ARL6 TRIM32 IFT27 BBS7 TTC8 INPP5E BBS10 BBS12 C8orf37
More info about this panelBBS16/SDCCAG8 single gene seq Panel
By Molecular Vision Laboratory
This panel specifically test the SDCCAG8 gene.
More info about this panelMVL Vision Panel Panel
By Molecular Vision Laboratory MVL Vision Panel that also includes the following genes: RGS9 RHO GRK1 RLBP1 ROM1 RP1 RP2 RP9 RPE65 RPGR
More info about this panelInvitae Senior-Loken Syndrome Panel Panel
By Invitae Invitae Senior-Loken Syndrome Panel that also includes the following genes: SDCCAG8 INVS WDR19 NPHP4 IQCB1 CEP290 NPHP1 NPHP3
More info about this panelInvitae Bardet-Biedl Syndrome Panel Panel
By Invitae Invitae Bardet-Biedl Syndrome Panel that also includes the following genes: SDCCAG8 ARL6 TRIM32 BBS7 TTC8 BBS10 BBS12 WDPCP CEP290 BBS9
More info about this panelInvitae Nephronophthisis Panel Panel
By Invitae Invitae Nephronophthisis Panel that also includes the following genes: SDCCAG8 NEK8 TMEM237 ZNF423 INVS CEP83 DCDC2 WDR19 NPHP4 AHI1
More info about this panelInvitae Ciliopathies Panel Panel
By Invitae Invitae Ciliopathies Panel that also includes the following genes: RPGR SDCCAG8 SPAG1 CEP41 RSPH1 CFAP298 ARL6 NEK8 IFT122 TMEM237
More info about this panelBardet-Biedl syndrome Panel
By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases Bardet-Biedl syndrome that also includes the following genes: SDCCAG8 ARL6 TRIM32 BBS7 TTC8 BBS10 BBS12 WDPCP BBIP1 CEP290
More info about this panelNephronophthisis Panel
By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases Nephronophthisis that also includes the following genes: SDCCAG8 NEK8 INVS NPHP4 AHI1 ANKS6 IQCB1 CEP290 RPGRIP1L GLIS2
More info about this panelBardet-Biedl Syndrome: Sequencing Panel Panel
By EGL Genetic Diagnostics Eurofins Clinical Diagnostics Bardet-Biedl Syndrome: Sequencing Panel that also includes the following genes: SDCCAG8 ARL6 TRIM32 BBS7 TTC8 BBS10 BBS12 WDPCP CEP290 BBS9
More info about this panelEye Disorders: Comprehensive Sequencing Panel Panel
By EGL Genetic Diagnostics Eurofins Clinical Diagnostics Eye Disorders: Comprehensive Sequencing Panel that also includes the following genes: RGS9 RHO RLBP1 ROM1 RP1 RP2 RP9 RPE65 RPGR RS1
More info about this panelSenior-Loken Syndrome: Sequencing and Deletion/Duplication Panel Panel
By EGL Genetic Diagnostics Eurofins Clinical Diagnostics Senior-Loken Syndrome: Sequencing and Deletion/Duplication Panel that also includes the following genes: SDCCAG8 INVS NPHP4 IQCB1 CEP290 NPHP1 NPHP3
More info about this panelCiliopathies: Sequencing Panel Panel
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 panelCongenital Obesity: Sequencing Panel Panel
By EGL Genetic Diagnostics Eurofins Clinical Diagnostics Congenital Obesity: Sequencing Panel that also includes the following genes: SDCCAG8 SIM1 ARL6 TRIM32 PHF6 BBS7 TTC8 VPS13B BBS10 BBS12
More info about this panelBardet-Biedl Syndrome: Deletion/Duplication Panel Panel
By EGL Genetic Diagnostics Eurofins Clinical Diagnostics Bardet-Biedl Syndrome: Deletion/Duplication Panel that also includes the following genes: SDCCAG8 ARL6 TRIM32 BBS7 TTC8 BBS10 BBS12 WDPCP CEP290 BBS9
More info about this panelCiliopathies: Deletion/Duplication Panel Panel
By EGL Genetic Diagnostics Eurofins Clinical Diagnostics Ciliopathies: Deletion/Duplication Panel that also includes the following genes: RPE65 RPGR ATXN10 SDCCAG8 TSC1 TSC2 TULP1 UMOD USH1C USH2A
More info about this panelEye Disorders: Deletion/Duplication Panel Panel
By EGL Genetic Diagnostics Eurofins Clinical Diagnostics Eye Disorders: Deletion/Duplication Panel that also includes the following genes: RGS9 RHO RLBP1 ROM1 RP1 RP2 RP9 RPE65 RPGR RS1
More info about this panelCiliopathies NGS Panel Panel
By Fulgent Genetics Fulgent Genetics Ciliopathies NGS Panel that also includes the following genes: RPE65 RPGR ATXN10 SDCCAG8 TULP1 UMOD USH1C USH2A CLRN1 VHL
More info about this panelBardet-Biedl Syndrome NGS Panel Panel
By Fulgent Genetics Fulgent Genetics Bardet-Biedl Syndrome NGS Panel that also includes the following genes: SDCCAG8 ARL6 TRIM32 BBS7 TTC8 BBS10 BBS12 WDPCP CEP290 BBS9
More info about this panelDiabetes-Obesity NGS Panel Panel
By Fulgent Genetics Fulgent Genetics Diabetes-Obesity NGS Panel that also includes the following genes: BDNF SDCCAG8 SIM1 HNF1A HNF1B WFS1 ARL6 NEUROG3 TRIM32 CEL
More info about this panelIntellectual Disability NGS Panel Panel
By Fulgent Genetics Fulgent Genetics Intellectual Disability NGS Panel that also includes the following genes: BCS1L RPS6KA3 SACS BIN1 SCN1A SCN8A SDCCAG8 SGCA SGSH ST3GAL3
More info about this panelNephronophthisis NGS Panel Panel
By Fulgent Genetics Fulgent Genetics Nephronophthisis NGS Panel that also includes the following genes: SDCCAG8 NEK8 INVS NPHP4 IQCB1 CEP290 RPGRIP1L GLIS2 NPHP1 NPHP3
More info about this panelSenior-Loken Syndrome NGS Panel Panel
By Fulgent Genetics Fulgent Genetics Senior-Loken Syndrome NGS Panel that also includes the following genes: SDCCAG8 NPHP4 CEP290 NPHP1 NPHP3
More info about this panelSDCCAG8 Panel
By Fulgent Genetics Fulgent Genetics
This panel specifically test the SDCCAG8 gene.
More info about this panelKidneySeq - 264 Genes Panel
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 panelSenior-Loken Syndrome Panel Panel
By Blueprint Genetics Senior-Loken Syndrome Panel that also includes the following genes: SDCCAG8 TRAF3IP1 INVS NPHP4 IQCB1 CEP290 NPHP1 NPHP3
More info about this panelNephronophthisis Panel Panel
By Blueprint Genetics Nephronophthisis Panel that also includes the following genes: SDCCAG8 NEK8 ZNF423 INVS CEP83 DCDC2 WDR19 NPHP4 TTC21B ANKS6
More info about this panelMonogenic Obesity Panel Panel
By Blueprint Genetics Monogenic Obesity Panel that also includes the following genes: SDCCAG8 SIM1 UCP3 ARL6 TRIM32 PHF6 KSR2 BBS7 TTC8 VPS13B
More info about this panelCystic Kidney Disease Panel Panel
By Blueprint Genetics Cystic Kidney Disease Panel that also includes the following genes: SDCCAG8 SIX5 HNF1B TSC1 TSC2 UMOD VHL NEK8 ZNF423 INVS
More info about this panelRetinal Dystrophy Panel Panel
By Blueprint Genetics Retinal Dystrophy Panel that also includes the following genes: RGS9 RHO RLBP1 ROM1 RP1 RP2 RPE65 RPGR RS1 CNNM4
More info about this panelCiliopathy Panel Panel
By Blueprint Genetics Ciliopathy Panel that also includes the following genes: SDCCAG8 CEP41 CFAP410 USP9X ZIC3 ARL6 NEK8 IFT122 IFT81 TMEM237
More info about this panelBardet-Biedl Syndrome Panel Panel
By Blueprint Genetics Bardet-Biedl Syndrome Panel that also includes the following genes: SDCCAG8 ARL6 PNPLA6 TRIM32 BBS7 TTC8 BBS10 BBS12 C8orf37 WDPCP
More info about this panelBARDET-BIEDL SYNDROME (NGS) Panel
By Laboratorio de Genetica Clinica SL BARDET-BIEDL SYNDROME (NGS) that also includes the following genes: SDCCAG8 ARL6 TRIM32 IFT27 BBS7 TTC8 BBS10 BBS12 WDPCP BBIP1
More info about this panelNEPHRONOPHTHISIS NGS PANEL Panel
By Laboratorio de Genetica Clinica SL NEPHRONOPHTHISIS NGS PANEL that also includes the following genes: SDCCAG8 ARL6 NEK8 ZNF423 INVS CEP83 WDR19 NPHP4 TTC21B ANKS6
More info about this panelSENIOR-LOKEN SYNDROME NGS PANEL Panel
By Laboratorio de Genetica Clinica SL SENIOR-LOKEN SYNDROME NGS PANEL that also includes the following genes: SDCCAG8 TRAF3IP1 INVS WDR19 NPHP4 IQCB1 CEP290 CEP164 NPHP1 NPHP3
More info about this panelBardet-Biedl Syndrome , Panel Massive Sequencing (NGS) 18 Genes Panel
By Reference Laboratory Genetics Bardet-Biedl Syndrome , Panel Massive Sequencing (NGS) 18 Genes that also includes the following genes: SDCCAG8 ARL6 TRIM32 BBS7 TTC8 BBS10 BBS12 WDPCP BBIP1 CEP290
More info about this panelNephronophthisis , Panel Massive Sequencing (NGS) 11 Genes Panel
By Reference Laboratory Genetics Nephronophthisis , Panel Massive Sequencing (NGS) 11 Genes that also includes the following genes: SDCCAG8 NEK8 INVS NPHP4 AHI1 IQCB1 CEP290 RPGRIP1L GLIS2 NPHP1
More info about this panelSenior-Loken Syndrome , Panel Massive Sequencing (NGS) 7 Genes Panel
By Reference Laboratory Genetics Senior-Loken Syndrome , Panel Massive Sequencing (NGS) 7 Genes that also includes the following genes: SDCCAG8 TRAF3IP1 WDR19 NPHP4 IQCB1 CEP290 NPHP1
More info about this panelSyndromic Hirschsprung Disease: gene sequencing panel Panel
By CEN4GEN Institute for Genomics and Molecular Diagnostics Syndromic Hirschsprung Disease: gene sequencing panel that also includes the following genes: BDNF SDCCAG8 SOX10 ARL6 ZEB2 TRIM32 BBS7 TTC8 KIF1BP BBS10
More info about this panelBardet-Biedl Syndrome: gene sequencing panel Panel
By CEN4GEN Institute for Genomics and Molecular Diagnostics Bardet-Biedl Syndrome: gene sequencing panel that also includes the following genes: SDCCAG8 ARL6 TRIM32 IFT27 BBS7 TTC8 BBS10 BBS12 WDPCP BBIP1
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