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| Term | autosomal recessive spinocerebellar ataxia 22 | ID (Ontology) | DOID:0111614 (Human Disease) |
| Definition | An autosomal recessive cerebellar ataxia that has_material_basis_in homozygous or compound heterozygous mutation in the VWA3B gene on chromosome 2q11.2. | ||
| Also Known As | "SCAR22" | ||
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autosomal recessive disease__ cerebellar ataxia____________| autosomal recessive cerebellar ataxia |__autosomal recessive spinocerebellar ataxia 22 |
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| Is a | autosomal recessive cerebellar ataxia | ||
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| MIM:616948 | |||