Dystonia 25
Disease ID: disease_node_17278
Connections displayed (default: 10).
Loading graph...
| Dbxref | ICD10CM:G24.1, MIM:615073, ORDO:329466 |
|---|---|
| Subclassof | DOID_0050736, DOID_0050837 |
| Data Source | DOID |
| Doid Label | dystonia 25 |
| Doid Description | A multifocal dystonia that is characterized by cervical, laryngeal and hand-forearm dystonia, and has_material_basis_in autosomal domit inheritance of heterozygous mutation in the GNAL gene on chromosome 18p11. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_17278 |
| Doid Id | DOID_0090055 |
| Label | Dystonia 25 |
- Outgoing r'ship
SUBCLASS_OFto/from Multifocal Dystonia(ID:disease_node_17277) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease)