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

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Path 1
Term Annotations click to browse term
  disease 14920
    disease of anatomical entity 14086
      nervous system disease 9150
        neurodegenerative disease 2536
          primary cerebellar degeneration 224
            autosomal recessive spinocerebellar ataxia 19 1
Path 2
Term Annotations click to browse term
  disease 14920
    disease of anatomical entity 14086
      nervous system disease 9150
        central nervous system disease 6948
          brain disease 6454
            movement disease 1006
              Dyskinesias 718
                Ataxia 308
                  hereditary ataxia 194
                    cerebellar ataxia 178
                      autosomal recessive cerebellar ataxia 69
                        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.