ONTOLOGY REPORT - ANNOTATIONS


Term:spinocerebellar ataxia type 37
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Accession:DOID:0050984 term browser browse the term
Definition:An autosomal dominant neurologic disorder characterized by adult onset of slowly progressive gait instability, frequent falls, and dysarthria associated with cerebellar atrophy on brain imaging. (OMIM)
Synonyms:exact_synonym: SCA37;   spinocerebellar ataxia 37
 primary_id: OMIM:615945
 alt_id: RDO:9001772
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spinocerebellar ataxia type 37 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Dab1 DAB adaptor protein 1 JBrowse link 5 123,154,360 124,279,170 RGD:8554872
RGD:7240710

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14926
    disease of anatomical entity 14092
      nervous system disease 9154
        neurodegenerative disease 2536
          hereditary ataxia 194
            autosomal dominant cerebellar ataxia 62
              spinocerebellar ataxia type 37 1
Path 2
Term Annotations click to browse term
  disease 14926
    disease of anatomical entity 14092
      nervous system disease 9154
        central nervous system disease 6950
          brain disease 6456
            movement disease 1006
              Dyskinesias 718
                Ataxia 308
                  hereditary ataxia 194
                    cerebellar ataxia 178
                      autosomal dominant cerebellar ataxia 62
                        spinocerebellar ataxia type 37 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.