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
|