| Metadata | |
|---|---|
| ID | DOID:0090037 |
| Name | torsion dystonia 13 |
| Definition | A dystonia that is characterized by focal or segmental dystonia with cranial, cervical, or upper limb involvement that has_material_basis_in autosomal dominant inheritance of variation in the chromosome region 1p36.32-p36.13. https://www.ncbi.nlm.nih.gov/pubmed/11261511, https://www.omim.org/entry/607671 |
| Xrefs | |
| Subsets |
DO_rare_slim |
| Parent Relationships |
is_a autosomal dominant disease is_a dystonia |
| Subclass Logical Relationships |
has material basis in some autosomal dominant inheritance |