Disease #04389 (DYT23 (dystonia?, type 23 (DYT-23)), OMIM:614860)
| Official abbreviation |
DYT23 |
| Name |
dystonia?, type 23 (DYT-23) |
| OMIM ID |
614860 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
CACNA1B |
| 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) |
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