Autosomal Recessive Spinocerebellar Ataxia 32
Disease ID: disease_node_16024
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| Dbxref | MIM:619862 |
|---|---|
| Subclassof | DOID_0050950 |
| Data Source | DOID |
| Synonyms | SCAR32 |
| Doid Label | autosomal recessive spinocerebellar ataxia 32 |
| Doid Description | An autosomal recessive cerebellar ataxia characterized by onset of gait ataxia in the second or third decade of life that has_material_basis_in homozygous or compound heterozygous mutation in the PRDX3 gene on chromosome 10q26. |
| Disease Node Id | disease_node_16024 |
| Doid Id | DOID_0070413 |
| Label | Autosomal Recessive Spinocerebellar Ataxia 32 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Cerebellar Ataxia(ID:disease_node_16008) (Disease)