Torsion Dystonia 13
Disease ID: disease_node_14351
Connections displayed (default: 10).
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| Dbxref | ICD10CM:G24.1, MIM:607671, ORDO:98807 |
|---|---|
| Subclassof | DOID_0050736, DOID_543 |
| Data Source | DOID |
| Doid Label | torsion dystonia 13 |
| Doid Description | A dystonia that is characterized by focal or segmental dystonia with cranial, cervical, or upper limb involvement that has_material_basis_in autosomal domit inheritance of variation in the chromosome region 1p36.32-p36.13. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_14351 |
| Doid Id | DOID_0090037 |
| Label | Torsion Dystonia 13 |
- Outgoing r'ship
SUBCLASS_OFto/from Dystonia(ID:disease_node_2684) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease)