Disease #03822 (DYT25 (dystonia, type 25 (DYT-25)), OMIM:615073)
Official abbreviation |
DYT25 |
Name |
dystonia, type 25 (DYT-25) |
OMIM ID |
615073 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
GNAL |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
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