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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:Corneal Dystrophy, Fuchs Endothelial, 7
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Accession:DOID:9001320 term browser browse the term
Synonyms:exact_synonym: CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, LATE-ONSET;   FCD4 LOCUS;   FECD7
 primary_id: MESH:C567674
 alt_id: OMIM:613271
For additional species annotation, visit the Alliance of Genome Resources.


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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 20983
    sensory system disease 7131
      eye disease 3308
        corneal disease 213
          corneal dystrophy 51
            corneal endothelial dystrophy 10
              Fuchs' endothelial dystrophy 9
                Corneal Dystrophy, Fuchs Endothelial, 7 0
Path 2
Term Annotations click to browse term
  disease 20983
    Pathological Conditions, Signs and Symptoms 13307
      Signs and Symptoms 10863
        Neurologic Manifestations 10111
          sensory system disease 7131
            eye disease 3308
              Hereditary Eye Diseases 1076
                corneal dystrophy 51
                  corneal endothelial dystrophy 10
                    Fuchs' endothelial dystrophy 9
                      Corneal Dystrophy, Fuchs Endothelial, 7 0
paths to the root