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| Term | ataxia with oculomotor apraxia type 3 | ID (Ontology) | DOID:0060557 (Human Disease) |
| Definition | An autosomal recessive cerebellar ataxia that is characterized by poor coordination and balance (ataxia) that worsen over time and that has_material_basis_in homozygous mutation in the PIK3R5 gene on chromosome 17p13. | ||
| Also Known As | "ataxia-oculomotor apraxia 3" | ||
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autosomal recessive disease__ cerebellar ataxia____________| autosomal recessive cerebellar ataxia |__ataxia with oculomotor apraxia type 3 |
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| Is a | autosomal recessive cerebellar ataxia | ||
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| MIM:615217 | |||