autosomal dominant nocturnal frontal lobe epilepsy
Information
- Disease name
- autosomal dominant nocturnal frontal lobe epilepsy
- Disease ID
- DOID:0060681
- Description
- "A frontal lobe epilepsy that is characterized by autosomal dominant inheritance with childhood onset of clusters of brief nocturnal motor seizures with hyperkinetic or tonic manifestations." [url:https\://www.ncbi.nlm.nih.gov/pubmed/7895015]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
- Disase is a (Disease Ontology)
- DOID:3331
- Cross Reference ID (Disease Ontology)
- GARD:11918
- Cross Reference ID (Disease Ontology)
- MESH:C579932
- Cross Reference ID (Disease Ontology)
- MIM:PS600513
- Cross Reference ID (Disease Ontology)
- ORDO:98784
- Exact Synonym (Disease Ontology)
- ENFL
- OrphaNumber from OrphaNet (Orphanet)
- 98784