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RGD uses the Human Disease Ontology (DO, 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:MERRF/MELAS Overlap Syndrome
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Accession:DOID:9003712 term browser browse the term
Definition:A mitochondrial encephalomyopathy which features symptoms of either MERFF or MELAS Syndrome or both.
For additional species annotation, visit the Alliance of Genome Resources.

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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 18256
    syndrome 9802
      MERRF Syndrome 3
        MERRF/MELAS Overlap Syndrome 0
Path 2
Term Annotations click to browse term
  disease 18256
    disease of anatomical entity 17617
      nervous system disease 13267
        peripheral nervous system disease 3065
          neuropathy 2847
            neuromuscular disease 2237
              muscular disease 1465
                muscle tissue disease 959
                  myopathy 787
                    mitochondrial myopathy 111
                      mitochondrial encephalomyopathy 68
                        MELAS syndrome 15
                          MERRF/MELAS Overlap Syndrome 0
paths to the root