OBO ID: DOID:0060730 |
Term Name: | torsion dystonia 1 | Search Ontology: | |
---|---|---|---|
Synonyms: |
|
||
Definition: | A generalized dystomia characterized by autosomal dominant inheritance of dystonia usually presenting initially as focal, typically in the limbs, but often generalizes with age that has_material_basis_in heterozygous mutation in the TOR1A gene on chromosome 9q34. (2) | ||
References: |
|
||
Ontology: | Human Disease ( DOID:0060730 ) |
OTHER torsion dystonia 1 PAGES
GENES INVOLVED
Human Gene | Zebrafish Ortholog | OMIM Term | OMIM Phenotype ID |
---|---|---|---|
TOR1A | Dystonia-1, torsion |
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
Your Input Welcome
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if
additional information is required.
Oops. Something went wrong. Please try again later.