Disease #06497 (LEUDEN (Leukoencephalopathy, developmental delay, and episodic neurologic regression syndrome), OMIM:618877)
| Official abbreviation |
LEUDEN |
| Name |
Leukoencephalopathy, developmental delay, and episodic neurologic regression syndrome |
| OMIM ID |
618877 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
EIF2AK2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2021-12-10 23:20:41 +01:00 (CET) |
| Date last edited |
N/A |
Individuals
|