Disease #07073 (NEDEGE (neurodevelopmental disorder with or without early-onset generalized epilepsy), OMIM:619157)
| Official abbreviation |
NEDEGE |
| Name |
neurodevelopmental disorder with or without early-onset generalized epilepsy |
| OMIM ID |
619157 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
NBEA |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2024-03-16 11:48:42 +01:00 (CET) |
| Date last edited |
N/A |
Individuals
|