autosomal dominant nocturnal frontal lobe epilepsy 5
Information
- Disease name
- autosomal dominant nocturnal frontal lobe epilepsy 5
- Disease ID
- DOID:0060686
- Description
- "An autosomal dominant nocturnal frontal lobe epilepsy that has_material_basis_in heterozygous mutation in the KCNT1 gene on chromosome 9q34." [url:https\://www.ncbi.nlm.nih.gov/pubmed/23086396]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
- Disase is a (Disease Ontology)
- DOID:0060681
- Cross Reference ID (Disease Ontology)
- MIM:615005
- Exact Synonym (Disease Ontology)
- ENFL5
- Exact Synonym (Disease Ontology)
- nocturnal frontal lobe epilepsy 5