WormBase Tree Display for DO_term: DOID:0080060
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DOID:0080060 | Name | autosomal recessive spinocerebellar ataxia 12 | |||
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Status | Valid | ||||
Definition | An 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. | ||||
Synonym | Exact | SCAR12 | |||
Parent | Is_a | DOID:0050950 | |||
DB_info | Database | OMIM | disease | 614322 | |
Attribute_of | Gene_by_orthology | WBGene00000971 | |||
WBGene00000972 | |||||
WBGene00010762 | |||||
WBGene00017082 | |||||
WBGene00017131 | |||||
WBGene00017971 |