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
|