Disease #06642 (EIEE78 (Epileptic encephalopathy, early infantile, 78), OMIM:618557)
Official abbreviation |
EIEE78 |
Name |
Epileptic encephalopathy, early infantile, 78 |
OMIM ID |
618557 |
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 |
GABRA2 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2021-12-10 23:20:41 +01:00 (CET) |
Date last edited |
N/A |
Individuals
|
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