G2Cdb::Human Disease report
- Disease id
- D00000197
- Name
- Epilepsy (autosomal dominant lateral temporal)
- Nervous system disease
- yes
Genes (1)
| Gene | Name/Description | Mutations Found | Literature | Mutations Type | Genetic association? |
|---|---|---|---|---|---|
| G00001881 | L1CAM L1 cell adhesion molecule |
Y | (17296837) | Single nucleotide polymorphism (SNP) | Y |
| G00001881 | L1CAM L1 cell adhesion molecule |
Y | (17296837) | Single nucleotide polymorphism (SNP) | Y |