OFD1 - orofaciodigital syndrome type 1
This test is available for the following conditions:
- Conditions > Intellectual Disability > Orofaciodigital syndrome
- Conditions > Multiple congenital anomalies (MCA) > Orofaciodigital syndrome
- Conditions > Hearing impairment > Orofaciodigital syndrome
- Conditions > Skeletal > Orofaciodigital syndrome
This product is also part of the following panels:
- Ciliopathies panel
- Craniofacial anomalies panel
- Epilepsy panel
- Intellectual disability panel
- Mendelian inherited disorders panel
- Orofacial clefting panel
- Renal disorders panel
- Short stature/skeletal dysplasia panel
- Skin disorders panel¹
- 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:
311200
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane