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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:Leigh Syndrome due to Mitochondrial Complex III Deficiency
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Accession:DOID:9000679 term browser browse the term
Synonyms:primary_id: MESH:C564962

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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 16063
    Nutritional and Metabolic Diseases 6696
      disease of metabolism 6696
        Metabolic Brain Diseases 1359
          Metabolic Brain Diseases, Inborn 1240
            Leigh disease 169
              Leigh Syndrome due to Mitochondrial Complex III Deficiency 0
Path 2
Term Annotations click to browse term
  disease 16063
    Developmental Disease 15996
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 15949
        genetic disease 15939
          inherited metabolic disorder 5144
            carbohydrate metabolic disorder 2528
              Pyruvate Metabolism, Inborn Errors 245
                Leigh disease 169
                  Leigh Syndrome due to Mitochondrial Complex III Deficiency 0
paths to the root