Epilepsy with auditory features
| Disease Term | Disease ID | Gene Symbol | Classification | References | Source |
|---|---|---|---|---|---|
| Autosomal dominant epilepsy with auditory features | 101046 | LGI1 | Causal Pathogenic evidence from ClinVar | - | ClinVar |
| DEPDC5 | Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations | - | - | ||
| RELN | Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations | - | - |