Autosomal Recessive Spinocerebellar Ataxia 22
Disease ID: disease_node_16011
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| Dbxref | MIM:616948 |
|---|---|
| Subclassof | DOID_0050950 |
| Data Source | DOID |
| Synonyms | SCAR22 |
| Doid Label | autosomal recessive spinocerebellar ataxia 22 |
| Doid Description | An autosomal recessive cerebellar ataxia that has_material_basis_in homozygous or compound heterozygous mutation in the VWA3B gene on chromosome 2q11.2. |
| Disease Node Id | disease_node_16011 |
| Doid Id | DOID_0111614 |
| Label | Autosomal Recessive Spinocerebellar Ataxia 22 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Cerebellar Ataxia(ID:disease_node_16008) (Disease)