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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:Peroxisome Biogenesis Disorder, Complementation Group 12
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Accession:DOID:9003612 term browser browse the term
Synonyms:primary_id: MESH:C566405


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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 21128
    Nutritional and Metabolic Diseases 8237
      disease of metabolism 8237
        inherited metabolic disorder 6214
          peroxisomal disease 344
            peroxisomal biogenesis disorder 250
              Peroxisome Biogenesis Disorder, Complementation Group 12 0
Path 2
Term Annotations click to browse term
  disease 21128
    Developmental Disease 18449
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 18309
        genetic disease 18253
          inherited metabolic disorder 6214
            peroxisomal disease 344
              peroxisomal biogenesis disorder 250
                Peroxisome Biogenesis Disorder, Complementation Group 12 0
paths to the root