NL
Complement mediated renal disease panel
This test is available for the following conditions:
- Conditions > Complement-mediated diseases > Complement-mediated kidney disease
Turnaround time
Regular: 2-3 months / Rapid: 15 working days
Method
- Exome analysis (WES or WGS data)
Panel version:
DG-4.2.0
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood (preferably), isolated DNA (only when EDTA blood is not an option)
C3 - complement-mediated kidney disease
This test is available for the following conditions:
- Conditions > Complement-mediated diseases > Complement-mediated kidney disease
This product is also part of the following panels:
- Complement mediated renal disease panel
- Comprehensive preconception carrier test panel¹
- Hemostatic/thrombotic disorders panel
- Mendelian inherited disorders panel with genome wide CNV analysis
- Primary immunodeficiencies panel
- Renal disorders panel
Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Method
- Sequence analysis of all coding exons and flanking intron-exon boundaries
OMIM:
120700
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane
CFB - complement-mediated kidney disease
This test is available for the following conditions:
- Conditions > Complement-mediated diseases > Complement-mediated kidney disease
This product is also part of the following panels:
- Complement mediated renal disease panel
- Hemostatic/thrombotic disorders panel
- Mendelian inherited disorders panel with genome wide CNV analysis
- Primary immunodeficiencies panel
- Renal disorders panel
Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Method
- Sequence analysis of all coding exons and flanking intron-exon boundaries
OMIM:
138470
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane
CFH - complement-mediated kidney disease
This test is available for the following conditions:
- Conditions > Complement-mediated diseases > Complement-mediated kidney disease
This product is also part of the following panels:
- Complement mediated renal disease panel
- Comprehensive preconception carrier test panel¹
- Hemostatic/thrombotic disorders panel
- Mendelian inherited disorders panel with genome wide CNV analysis
- Primary immunodeficiencies panel
- Renal disorders panel
- Vision disorders panel
Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Method
- Sequence analysis of all coding exons and flanking intron-exon boundaries
OMIM:
134370
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane
CFHR1 - complement-mediated kidney disease
This test is available for the following conditions:
- Conditions > Complement-mediated diseases > Complement-mediated kidney disease
This product is also part of the following panels:
- Complement mediated renal disease panel
- Mendelian inherited disorders panel with genome wide CNV analysis
- Renal disorders panel
Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Method
- Sequence analysis of all coding exons and flanking intron-exon boundaries
OMIM:
134371
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane
CFHR2 - complement-mediated kidney disease
This test is available for the following conditions:
- Conditions > Complement-mediated diseases > Complement-mediated kidney disease
This product is also part of the following panels:
- Complement mediated renal disease panel
- Mendelian inherited disorders panel with genome wide CNV analysis
Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Method
- Sequence analysis of all coding exons and flanking intron-exon boundaries
OMIM:
600889
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane
CFHR3 - complement-mediated kidney disease
This test is available for the following conditions:
- Conditions > Complement-mediated diseases > Complement-mediated kidney disease
This product is also part of the following panels:
- Complement mediated renal disease panel
- Mendelian inherited disorders panel with genome wide CNV analysis
- Renal disorders panel
Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Method
- Sequence analysis of all coding exons and flanking intron-exon boundaries
OMIM:
605336
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane
CFHR4 - complement-mediated kidney disease
This test is available for the following conditions:
- Conditions > Complement-mediated diseases > Complement-mediated kidney disease
This product is also part of the following panels:
- Complement mediated renal disease panel
- Mendelian inherited disorders panel with genome wide CNV analysis
Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Method
- Sequence analysis of all coding exons and flanking intron-exon boundaries
OMIM:
605337
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane
CFHR5 - complement-mediated kidney disease
This test is available for the following conditions:
- Conditions > Complement-mediated diseases > Complement-mediated kidney disease
This product is also part of the following panels:
- Complement mediated renal disease panel
- Mendelian inherited disorders panel with genome wide CNV analysis
- Renal disorders panel
Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Method
- Sequence analysis of all coding exons and flanking intron-exon boundaries
OMIM:
608593
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane
DGKE - complement-mediated kidney disease
This test is available for the following conditions:
- Conditions > Complement-mediated diseases > Complement-mediated kidney disease
This product is also part of the following panels:
- Complement mediated renal disease panel
- Comprehensive preconception carrier test panel¹
- Hemostatic/thrombotic disorders panel
- Mendelian inherited disorders panel with genome wide CNV analysis
- Metabolic disorders panel
- Renal disorders panel
Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Method
- Sequence analysis of all coding exons and flanking intron-exon boundaries
OMIM:
601440
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane
MCP - complement-mediated kidney disease
This test is available for the following conditions:
- Conditions > Complement-mediated diseases > Complement-mediated kidney disease
Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Method
- Sequence analysis of all coding exons and flanking intron-exon boundaries
OMIM:
120920
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane
THBD - complement-mediated kidney disease
This test is available for the following conditions:
- Conditions > Complement-mediated diseases > Complement-mediated kidney disease
This product is also part of the following panels:
- Complement mediated renal disease panel
- Hemostatic/thrombotic disorders panel
- Mendelian inherited disorders panel with genome wide CNV analysis
- Primary immunodeficiencies panel
- Renal disorders panel
Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Method
- Sequence analysis of all coding exons and flanking intron-exon boundaries
OMIM:
188040
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane
CFH operon - complement-mediated kidney disease (MLPA)
This test is available for the following conditions:
- Conditions > Complement-mediated diseases > Complement-mediated kidney disease
Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Method
- Deletion/duplication analysis (MLPA)
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane
