Severe myoclonic epilepsy in infancy
Information
- Disease name
- Severe myoclonic epilepsy in infancy
- Disease ID
- Description
Disease area statistics
Chromosome band
| Gene symbol | Chromosome | Start | Stop | The number of variant |
|---|---|---|---|---|
| SCN2A | 2 | 165,239,434 | 165,392,310 | 8 |
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
- MedGen concept unique identifier (MedGen Concept name)
- C0751122
- MedGen unique identifier (MedGen Concept name)
- 148243