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ONTOLOGY REPORT - ANNOTATIONS


Term:myoclonic dystonia 26
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Accession:DOID:0090036 term browser browse the term
Definition:An autosomal dominant neurologic disorder characterized by onset of myoclonic jerks affecting the upper limbs in the first or second decade of life. (OMIM)
Synonyms:exact_synonym: DYT26
 primary_id: OMIM:616398
 alt_id: RDO:9001436
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myoclonic dystonia 26 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Kctd17 potassium channel tetramerization domain containing 17 JBrowse link 7 119,647,301 119,658,148 RGD:8554872
RGD:7240710

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15984
    disease of anatomical entity 15262
      nervous system disease 10752
        Neurologic Manifestations 3877
          Dyskinesias 776
            dystonia 125
              myoclonic dystonia 5
                myoclonic dystonia 26 1
Path 2
Term Annotations click to browse term
  disease 15984
    disease of anatomical entity 15262
      nervous system disease 10752
        central nervous system disease 8839
          brain disease 8128
            movement disease 1064
              Dyskinesias 776
                dystonia 125
                  myoclonic dystonia 5
                    myoclonic dystonia 26 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.