Hemimegalencephaly
Information
- Disease name
- Hemimegalencephaly
- Disease ID
- Description
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
| NCT ID | Status | Phase | Summary | Start date | Completion date |
|---|---|---|---|---|---|
| NCT02890641 | Recruiting | Genetic and Electrophysiologic Study in Focal Drug-resistant Epilepsies | December 12, 2015 | December 2030 | |
| NCT04344626 | Withdrawn | N/A | Use of a Tonometer to Identify Epileptogenic Lesions During Pediatric Epilepsy Surgery | July 16, 2018 | March 2023 |
- HPO Human Phenotype ID (Human Phenotype Ontology)
- HP:0007206
- OrphaNumber from OrphaNet (Orphanet)
- 99802
- MeSH unique ID (MeSH (Medical Subject Headings))
- D065705