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WormBase Tree Display for DO_term: DOID:0080060

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Name Class

DOID:0080060Nameautosomal recessive spinocerebellar ataxia 12
StatusValid
DefinitionAn autosomal recessive cerebellar ataxia that is characterized by onset of generalized seizures in infancy, delayed psychomotor development with mental retardation, and cerebellar ataxia and that has_material_basis_in homozygous mutation in the WWOX gene on chromosome 16q23.
SynonymExactSCAR12
ParentIs_aDOID:0050950
DB_infoDatabaseOMIMdisease614322
Attribute_ofGene_by_orthologyWBGene00000971
WBGene00000972
WBGene00010762
WBGene00017082
WBGene00017131
WBGene00017971