AGXT - Hyperoxaluria, primary type I

This test is available for the following conditions:

  • Conditions > Metabolic disorders > Hyperoxaluria

This product is also part of the following panels:

  • WES comprehensive preconception carrier test ¹
  • WES Mendelian inherited disorders (100.0% **)
  • WES metabolic disorders (100.0% **)
  • WES renal disorders (100.0% **)

** % of the coding region of this gene has a coverage of >20x. (Without % information : This is a non-coding gene for which coverage statistics could not be determined)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries

OMIM: 604285
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 725

Gene

AGXT - Hyperoxaluria, primary type I

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 725

AGXT - Hyperoxaluria, primary type I



€ 725
Gene

GRHPR - Hyperoxaluria type II

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 725

GRHPR - Hyperoxaluria type II



€ 725

GRHPR - Hyperoxaluria type II

This test is available for the following conditions:

  • Conditions > Metabolic disorders > Hyperoxaluria

This product is also part of the following panels:

  • WES comprehensive preconception carrier test ¹
  • WES Mendelian inherited disorders (81.7% **)
  • WES metabolic disorders (81.7% **)
  • WES renal disorders (81.7% **)

** % of the coding region of this gene has a coverage of >20x. (Without % information : This is a non-coding gene for which coverage statistics could not be determined)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries

OMIM: 604296
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 725
Gene

HOGA1 - Hyperoxaluria, primary type III

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 725

HOGA1 - Hyperoxaluria, primary type III



€ 725

HOGA1 - Hyperoxaluria, primary type III

This test is available for the following conditions:

  • Conditions > Metabolic disorders > Hyperoxaluria

This product is also part of the following panels:

  • WES comprehensive preconception carrier test ¹
  • WES Mendelian inherited disorders (99.1% **)
  • WES metabolic disorders (99.1% **)
  • WES renal disorders (99.1% **)

** % of the coding region of this gene has a coverage of >20x. (Without % information : This is a non-coding gene for which coverage statistics could not be determined)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries

OMIM: 613597
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 725