WormBase Tree Display for DO_term: DOID:0050882
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| DOID:0050882 | Name | spinocerebellar ataxia type 5 | |||
|---|---|---|---|---|---|
| Status | Valid | ||||
| Definition | An autosomal dominant cerebellar ataxia that is characterized by the early-onset of cerebellar signs and eye movement abnormalities with a very slow disease progression, and has_material_basis_in mutation in the SPTBN2 gene. | ||||
| Parent | Is_a | DOID:1441 | |||
| DB_info | Database | OMIM | disease | 600224 | |
| Attribute_of | Gene_by_orthology | WBGene00006803 |
