Autosomal Recessive Spinocerebellar Ataxia 13
Disease ID: disease_node_16033
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| Dbxref | MIM:614831 |
|---|---|
| Subclassof | DOID_0050950 |
| Data Source | DOID |
| Synonyms | SCAR13 |
| Doid Label | autosomal recessive spinocerebellar ataxia 13 |
| Doid Description | An autosomal recessive cerebellar ataxia that is characterized by delayed psychomotor development beginning in infancy and that has_material_basis_in homozygous mutation in the GRM1 gene on chromosome 6q24. |
| Disease Node Id | disease_node_16033 |
| Doid Id | DOID_0080062 |
| Label | Autosomal Recessive Spinocerebellar Ataxia 13 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Cerebellar Ataxia(ID:disease_node_16008) (Disease)