Van Der Woude Syndrome 2(VWS2) Explore Disorder's Alias
An Autosomal dominant mode(s) within the Oral disorders category
Candidate Gene Information
An Autosomal dominant mode(s) within the Oral disorders category
Reported Pathogenic variants
| S.No. | Name/GeneID | Description | Cytogentic Band | Gene Location on genomic DNA | Gene Length | Exons | Details | Gene Cross-References |
| 1 | GRHL3/57822 | grainyhead like transcription factor 3 | 1p36.11 | Chr1, NC_000001.11 (24319357..24364482) |
45126 nt | 19 | More... | OMIM gene gnomAD browser EnsEMBL GeneCards ClinGen gene |
| Variant Information | ||||||||
| Disorder Cross-References: Orphanet OMIM GARD GTR MedGen MalaCards EMBL-EBI OLS Monarch Initiative NORD | ||||||||
Patient care services
Clinical Symptoms & Disabilities
Prevalence
| Under development |