Disease #00533 (DYT3 (dystonia, torsion, X-linked, type 3 (DYT-3, Parkinsonism)), OMIM:314250)
| Official abbreviation |
DYT3 |
| Name |
dystonia, torsion, X-linked, type 3 (DYT-3, Parkinsonism) |
| OMIM ID |
314250 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
X-linked recessive |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
TAF1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-21 21:17:28 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|