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Namespace Prefixes

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Statements

Subject Item

_:vb50945154

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n4:IAO_0000115

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An autosomal recessive cerebellar ataxia characterized by spinocerebellar ataxia with optic and cochlear degeneration that has_material_basis_in homozygous or compound heterozygous mutation in a region on chromosome 6p23-p21.

obo:hasDbXref

url:https://www.ncbi.nlm.nih.gov/pubmed/4154794 url:https://www.ncbi.nlm.nih.gov/pubmed/11175288 url:https://www.ncbi.nlm.nih.gov/pubmed/4434170