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RGD DISEASE ONTOLOGY - ANNOTATIONS

RGD uses the Human Disease Ontology (DO, https://disease-ontology.org/) for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.
Term:Mitochondrial Dystonia
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Accession:DOID:9003660 term browser browse the term
Synonyms:exact_synonym: maternally-inherited mitochondrial dystonia;   mitochondrial DNA-related dystonia;   mtDNA-related dystonia
 xref: ORDO:254851


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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 17773
    disease of anatomical entity 15145
      nervous system disease 13207
        Neurologic Manifestations 9572
          Dyskinesias 2123
            dystonia 426
              Mitochondrial Dystonia 0
Path 2
Term Annotations click to browse term
  disease 17773
    disease of anatomical entity 15145
      nervous system disease 13207
        central nervous system disease 11844
          brain disease 11124
            movement disease 2494
              Dyskinesias 2123
                dystonia 426
                  Mitochondrial Dystonia 0
paths to the root