Disease #04495 (DEE27 (encephalopathy, developmental and epileptic, type 27), OMIM:616139)
Official abbreviation |
DEE27 |
Name |
encephalopathy, developmental and epileptic, type 27 |
OMIM ID |
616139 |
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 |
GRIN2B |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2015-09-23 10:25:22 +02:00 (CEST) |
Date last edited |
2023-02-01 18:27:50 +01:00 (CET) |
Individuals
|