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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.
Synonyms:primary_id: RDO:9000710
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 17205
    syndrome 8125
      MERRF/MELAS Overlap Syndrome 0
Path 2
Term Annotations click to browse term
  disease 17205
    disease of anatomical entity 16551
      nervous system disease 12097
        peripheral nervous system disease 2533
          neuropathy 2330
            neuromuscular disease 1835
              muscular disease 1236
                muscle tissue disease 827
                  myopathy 661
                    mitochondrial myopathy 89
                      mitochondrial encephalomyopathy 48
                        MERRF Syndrome 3
                          MERRF/MELAS Overlap Syndrome 0
paths to the root