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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:exudative vitreoretinopathy 3
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Accession:DOID:0111409 term browser browse the term
Definition:An exudative vitreoretinopathy that has_material_basis_in heterozygous mutation in a region on chromosome 11p13-p12. (DO)
Synonyms:exact_synonym: EVR3
 primary_id: MESH:C565297
 alt_id: OMIM:605750


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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 17996
    sensory system disease 6633
      eye disease 3381
        Hereditary Eye Diseases 1081
          exudative vitreoretinopathy 22
            exudative vitreoretinopathy 3 0
Path 2
Term Annotations click to browse term
  disease 17996
    Pathological Conditions, Signs and Symptoms 12039
      Signs and Symptoms 9970
        Neurologic Manifestations 9647
          sensory system disease 6633
            eye disease 3381
              retinal disease 1175
                retinal vascular disease 197
                  exudative vitreoretinopathy 22
                    exudative vitreoretinopathy 3 0
paths to the root