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COD (Cerebroocular Dysgenesis) - Ontology Report - Rat Genome Database

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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:COD (Cerebroocular Dysgenesis)
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Accession:DOID:9004117 term browser browse the term
Synonyms:primary_id: MESH:C535631;   RDO:0000861

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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 19139
    syndrome 11404
      Walker-Warburg syndrome 71
        COD (Cerebroocular Dysgenesis) 0
Path 2
Term Annotations click to browse term
  disease 19139
    disease of anatomical entity 18451
      nervous system disease 14361
        peripheral nervous system disease 4399
          neuropathy 4187
            neuromuscular disease 3226
              muscular disease 2233
                muscle tissue disease 1358
                  myopathy 1049
                    muscular dystrophy 654
                      congenital muscular dystrophy 210
                        Walker-Warburg syndrome 71
                          COD (Cerebroocular Dysgenesis) 0
paths to the root