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ONTOLOGY REPORT - ANNOTATIONS


Term:autosomal recessive spinocerebellar ataxia 19
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Accession:DOID:0080065 term browser browse the term
Definition:An autosomal recessive neurologic disorder characterized by postnatal onset of severe progressive sensorineural hearing loss and progressive cerebellar ataxia. (OMIM)
Synonyms:exact_synonym: LICHTENSTEIN-KNORR SYNDROME;   LIKNS;   SCAR19
 primary_id: OMIM:616291;   RDO:9001633
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autosomal recessive spinocerebellar ataxia 19 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Slc9a1 solute carrier family 9 member A1 JBrowse link 5 151,573,122 151,626,360 RGD:7240710
RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15619
    disease of anatomical entity 14948
      nervous system disease 10216
        neurodegenerative disease 2691
          primary cerebellar degeneration 218
            autosomal recessive spinocerebellar ataxia 19 1
Path 2
Term Annotations click to browse term
  disease 15619
    disease of anatomical entity 14948
      nervous system disease 10216
        central nervous system disease 8092
          brain disease 7561
            movement disease 1000
              Dyskinesias 710
                Ataxia 300
                  hereditary ataxia 186
                    cerebellar ataxia 169
                      autosomal recessive cerebellar ataxia 58
                        autosomal recessive spinocerebellar ataxia 19 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.