Disease #05434 (IECEE1 (encephalopathy, epileptic, infantile or early childhood, type 1 ( IECEE-1)), OMIM:617711)
| Official abbreviation |
IECEE1 |
| Name |
encephalopathy, epileptic, infantile or early childhood, type 1 ( IECEE-1) |
| OMIM ID |
617711 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
2 |
| Phenotype entries for this disease |
2 |
| Associated with 1 gene |
PPP3CA |
| Associated tissues |
- |
| Disease features |
autosomal dominant |
| Remarks |
- |
| Date created |
2018-06-01 14:36:04 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|