ARID1B - autosomal dominant intellectual disability type 12
This test is available for the following conditions:
- Conditions > Intellectual Disability > Intellectual disability, autosomal dominant
- Conditions > Multiple congenital anomalies (MCA) > Intellectual disability, autosomal dominant
This product is also part of the following panels:
- WES epilepsy (99.3% **)
- WES intellectual disability (99.3% **)
- WES Mendelian inherited disorders (99.3% **)
- WES short stature/skeletal dysplasia (99.3% **)
- WES skin disorders¹ (99.3% **)
** % 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:
614556
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane
CTNNB1 - autosomal dominant intellectual disability with microcephaly and spasticity type 19
This test is available for the following conditions:
- Conditions > Intellectual Disability > Intellectual disability, autosomal dominant
- Conditions > Multiple congenital anomalies (MCA) > Intellectual disability, autosomal dominant
This product is also part of the following panels:
- WES intellectual disability (100.0% **)
- WES Mendelian inherited disorders (100.0% **)
- WES vision 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:
116806
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane
DEAF1 - autosomal dominant intellectual disability type 24
This test is available for the following conditions:
- Conditions > Intellectual Disability > Intellectual disability, autosomal dominant
- Conditions > Multiple congenital anomalies (MCA) > Intellectual disability, autosomal dominant
This product is also part of the following panels:
- WES comprehensive preconception carrier test ¹
- WES intellectual disability (99.1% **)
- WES Mendelian inherited 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:
602635
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane
DYNC1H1 - autosomal dominant intellectual disability type 13
This test is available for the following conditions:
- Conditions > Intellectual Disability > Intellectual disability, autosomal dominant
- Conditions > Multiple congenital anomalies (MCA) > Intellectual disability, autosomal dominant
This product is also part of the following panels:
- WES epilepsy (99.8% **)
- WES intellectual disability (99.8% **)
- WES Mendelian inherited disorders (99.8% **)
- WES muscle disorders (99.8% **)
- WES neuropathies (HMSN)¹ (99.8% **)
** % 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:
600112
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane
DYRK1A - autosomal dominant intellectual disability type 7
This test is available for the following conditions:
- Conditions > Intellectual Disability > Intellectual disability, autosomal dominant
- Conditions > Multiple congenital anomalies (MCA) > Intellectual disability, autosomal dominant
This product is also part of the following panels:
- WES epilepsy (100.0% **)
- WES intellectual disability (100.0% **)
- WES Mendelian inherited 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:
600855
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane
FOXP1 - intellectual disability with language impairment and autistic features
This test is available for the following conditions:
- Conditions > Intellectual Disability > Intellectual disability, autosomal dominant
- Conditions > Multiple congenital anomalies (MCA) > Intellectual disability, autosomal dominant
This product is also part of the following panels:
- WES intellectual disability (99.9% **)
- WES Mendelian inherited disorders (99.9% **)
** % 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:
605515
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane
GATAD2B - autosomal dominant intellectual disability type 18
This test is available for the following conditions:
- Conditions > Intellectual Disability > Intellectual disability, autosomal dominant
- Conditions > Multiple congenital anomalies (MCA) > Intellectual disability, autosomal dominant
This product is also part of the following panels:
- WES intellectual disability (99.6% **)
- WES Mendelian inherited disorders (99.6% **)
** % 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:
614998
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane
GRIN1 - autosomal dominant intellectual disability type 8
This test is available for the following conditions:
- Conditions > Intellectual Disability > Intellectual disability, autosomal dominant
- Conditions > Multiple congenital anomalies (MCA) > Intellectual disability, autosomal dominant
This product is also part of the following panels:
- WES comprehensive preconception carrier test ¹
- WES epilepsy (100.0% **)
- WES intellectual disability (100.0% **)
- WES Mendelian inherited disorders (100.0% **)
- WES movement disorders (100.0% **)
- WES muscle 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 & Targeted analysis: 12 weeks
Method
- Sequence analysis of all coding exons and flanking intron-exon boundaries
OMIM:
138249
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane
GRIN2B - autosomal dominant intellectual disability type 6
This test is available for the following conditions:
- Conditions > Intellectual Disability > Intellectual disability, autosomal dominant
- Conditions > Multiple congenital anomalies (MCA) > Intellectual disability, autosomal dominant
This product is also part of the following panels:
- WES epilepsy (99.2% **)
- WES intellectual disability (99.2% **)
- WES Mendelian inherited disorders (99.2% **)
- WES movement disorders (99.2% **)
** % 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:
138252
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane
KIF1A - autosomal dominant intellectual disability type 9
This test is available for the following conditions:
- Conditions > Intellectual Disability > Intellectual disability, autosomal dominant
- Conditions > Multiple congenital anomalies (MCA) > Intellectual disability, autosomal dominant
This product is also part of the following panels:
- WES comprehensive preconception carrier test ¹
- WES intellectual disability (98.2% **)
- WES Mendelian inherited disorders (98.2% **)
- WES mitochondrial disorders (98.2% **)
- WES movement disorders (98.2% **)
- WES neuropathies (HMSN)¹ (98.2% **)
** % 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:
601255
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane
MBD5 - autosomal dominant intellectual disability type 1
This test is available for the following conditions:
- Conditions > Intellectual Disability > Intellectual disability, autosomal dominant
- Conditions > Multiple congenital anomalies (MCA) > Intellectual disability, autosomal dominant
This product is also part of the following panels:
- WES epilepsy (99.8% **)
- WES intellectual disability (99.8% **)
- WES Mendelian inherited disorders (99.8% **)
** % 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:
611472
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane
MYT1L - autosomal dominant intellectual disability with obesity
This test is available for the following conditions:
- Conditions > Intellectual Disability > Intellectual disability, autosomal dominant
- Conditions > Multiple congenital anomalies (MCA) > Intellectual disability, autosomal dominant
This product is also part of the following panels:
- WES intellectual disability (99.9% **)
- WES Mendelian inherited disorders (99.9% **)
** % 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:
613084
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane
SMARCA4 - autosomal dominant intellectual disability type 16
This test is available for the following conditions:
- Conditions > Intellectual Disability > Intellectual disability, autosomal dominant
- Conditions > Multiple congenital anomalies (MCA) > Intellectual disability, autosomal dominant
This product is also part of the following panels:
- WES hereditary cancer (99.6% **)
- WES intellectual disability (99.6% **)
- WES Mendelian inherited disorders (99.6% **)
- WES short stature/skeletal dysplasia (99.6% **)
- WES skin disorders¹ (99.6% **)
** % 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:
603254
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane
SYNGAP1 - autosomal dominant intellectual disability type 5
This test is available for the following conditions:
- Conditions > Intellectual Disability > Intellectual disability, autosomal dominant
- Conditions > Multiple congenital anomalies (MCA) > Intellectual disability, autosomal dominant
This product is also part of the following panels:
- WES epilepsy (98.0% **)
- WES intellectual disability (98.0% **)
- WES Mendelian inherited disorders (98.0% **)
** % 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 & Targeted analysis: 12 weeks
Method
- Sequence analysis of all coding exons and flanking intron-exon boundaries
OMIM:
612621
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane
