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;   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

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Path 1
Term Annotations click to browse term
  disease 14926
    Developmental Diseases 7774
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7096
        genetic disease 6457
          myoclonic dystonia 26 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
                dystonia 80
                  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.