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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 Complex II Deficiency Nuclear Type 3
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Accession:DOID:9003007 term browser browse the term
Synonyms:exact_synonym: MC2DN3
 primary_id: OMIM:619167


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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 17996
    Nutritional and Metabolic Diseases 7184
      disease of metabolism 7184
        mitochondrial metabolism disease 808
          mitochondrial complex II deficiency 3
            Mitochondrial Complex II Deficiency Nuclear Type 3 0
Path 2
Term Annotations click to browse term
  disease 17996
    Developmental Disease 17885
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 17802
        genetic disease 17786
          inherited metabolic disorder 5521
            mitochondrial metabolism disease 808
              mitochondrial complex II deficiency 3
                Mitochondrial Complex II Deficiency Nuclear Type 3 0
paths to the root