Disease #04406 (EPM8 (epilepsy?, myoclonic, progressive, type 8 (EPM-8)), OMIM:616230)
| Official abbreviation |
EPM8 |
| Name |
epilepsy?, myoclonic, progressive, type 8 (EPM-8) |
| OMIM ID |
616230 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
2 |
| Phenotype entries for this disease |
2 |
| Associated with 1 gene |
CERS1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2015-09-23 10:25:22 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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