ONTOLOGY REPORT - ANNOTATIONS


Term:autosomal recessive spinocerebellar ataxia 10
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Accession:DOID:0050999 term browser browse the term
Definition:An autosomal recessive cerebellar ataxia that is characterized by ataxia, dysarthria, nystagmus and marked cerebellar atrophy, has_material_basis_in mutation in the ANO10 gene. (DO)
Synonyms:exact_synonym: SCAR10
 primary_id: OMIM:613728;   RDO:9000826
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autosomal recessive spinocerebellar ataxia 10 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Ano10 anoctamin 10 JBrowse link 8 130,812,941 130,931,021 RGD:7240710
RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14919
    disease of anatomical entity 14083
      nervous system disease 9147
        neurodegenerative disease 2534
          hereditary ataxia 193
            autosomal recessive cerebellar ataxia 68
              autosomal recessive spinocerebellar ataxia 10 1
Path 2
Term Annotations click to browse term
  disease 14919
    disease of anatomical entity 14083
      nervous system disease 9147
        central nervous system disease 6945
          brain disease 6451
            movement disease 1005
              Dyskinesias 717
                Ataxia 307
                  hereditary ataxia 193
                    cerebellar ataxia 177
                      autosomal recessive cerebellar ataxia 68
                        autosomal recessive spinocerebellar ataxia 10 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.