Disease #05710 (EIEE61 (encephalopathy, epileptic, early infantile, type 61 (EIEE61)), OMIM:617933)
| Official abbreviation |
EIEE61 |
| Name |
encephalopathy, epileptic, early infantile, type 61 (EIEE61) |
| OMIM ID |
617933 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
ADAM22 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2020-03-03 17:40:39 +01:00 (CET) |
| Date last edited |
N/A |
|