Disease #05788 (EIEE66 (encephalopathy, epileptic, early infantile, type 66 (EIEE66)), OMIM:618067)
| Official abbreviation |
EIEE66 |
| Name |
encephalopathy, epileptic, early infantile, type 66 (EIEE66) |
| OMIM ID |
618067 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
PACS2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2020-07-14 19:33:46 +02:00 (CEST) |
| Date last edited |
N/A |
Individuals
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