Disease #05774 (EIEE83 (encephalopathy, epileptic, early infantile, type 83 (EIEE83)), OMIM:618744)
| Official abbreviation |
EIEE83 |
| Name |
encephalopathy, epileptic, early infantile, type 83 (EIEE83) |
| OMIM ID |
618744 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
UGP2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2020-06-15 19:42:51 +02:00 (CEST) |
| Date last edited |
N/A |
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