Disease #05835 (EPRPDC (epilepsy, rolandic, with proxysmal exercise-induce dystonia and writer's cramp (EPRPDC)), OMIM:608105)
| Official abbreviation |
EPRPDC |
| Name |
epilepsy, rolandic, with proxysmal exercise-induce dystonia and writer's cramp (EPRPDC) |
| OMIM ID |
608105 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
TBC1D24 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2020-09-18 16:18:07 +02:00 (CEST) |
| Date last edited |
N/A |
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