Disease #06770 (EIEE76 (Epileptic encephalopathy, early infantile, 76), OMIM:618468)
| Official abbreviation |
EIEE76 |
| Name |
Epileptic encephalopathy, early infantile, 76 |
| OMIM ID |
618468 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
ACTL6B |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2021-12-10 23:20:41 +01:00 (CET) |
| Date last edited |
N/A |
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|