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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;   RDO:9001436
For additional species annotation, visit the Alliance of Genome Resources.


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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

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Path 1
Term Annotations click to browse term
  disease 14759
    Developmental Diseases 7628
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 6666
        genetic disease 5913
          myoclonic dystonia 26 1
Path 2
Term Annotations click to browse term
  disease 14759
    disease of anatomical entity 13978
      nervous system disease 9097
        central nervous system disease 6892
          brain disease 6396
            movement disease 989
              Dystonic Disorders 80
                dystonia 74
                  myoclonic dystonia 5
                    myoclonic dystonia 26 1
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