Disease #03139 (EPM1B (epilepsy, progressive myoclonic, type 1B (EPM1B)), OMIM:612437)
| Official abbreviation |
EPM1B |
| Name |
epilepsy, progressive myoclonic, type 1B (EPM1B) |
| OMIM ID |
612437 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
7 |
| Phenotype entries for this disease |
7 |
| Associated with 1 gene |
PRICKLE1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2021-03-02 12:20:06 +01:00 (CET) |
Individuals
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