Disease #00061 (Epilepsy)
Official abbreviation |
- |
Name |
Epilepsy |
OMIM ID |
- |
Inheritance |
- |
Individuals reported having this disease |
16 |
Phenotype entries for this disease |
3 |
Associated with 4 genes |
RORA, RORB, SCN2A, SCN2B |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Individuals
|
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