Autosomal Recessive Spinocerebellar Ataxia 10
Disease ID: disease_node_16040
Connections displayed (default: 10).
Loading graph...
| Dbxref | MIM:613728 |
|---|---|
| Subclassof | DOID_0050950 |
| Data Source | DOID |
| Synonyms | SCAR10 |
| Doid Label | autosomal recessive spinocerebellar ataxia 10 |
| Doid Description | An autosomal recessive cerebellar ataxia that is characterized by ataxia, dysarthria, nystagmus and marked cerebellar atrophy, has_material_basis_in mutation in the ANO10 gene. |
| Disease Node Id | disease_node_16040 |
| Doid Id | DOID_0050999 |
| Label | Autosomal Recessive Spinocerebellar Ataxia 10 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Cerebellar Ataxia(ID:disease_node_16008) (Disease)