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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, 2
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Accession:DOID:9005877 term browser browse the term
Synonyms:exact_synonym: FCD1 LOCUS;   FECD2;   Late-onset Fuchs' endothelial corneal dystrophy
 primary_id: MESH:C535479
 alt_id: OMIM:610158



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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 41189
    sensory system disease 9728
      eye disease 4940
        corneal disease 328
          corneal dystrophy 81
            corneal endothelial dystrophy 12
              Fuchs' endothelial dystrophy 11
                Corneal Dystrophy, Fuchs' Endothelial, 2 0
Path 2
Term Annotations click to browse term
  disease 41189
    Pathological Conditions, Signs and Symptoms 21466
      Signs and Symptoms 16320
        Neurologic Manifestations 15387
          sensory system disease 9728
            eye disease 4940
              Hereditary Eye Diseases 1623
                corneal dystrophy 81
                  corneal endothelial dystrophy 12
                    Fuchs' endothelial dystrophy 11
                      Corneal Dystrophy, Fuchs' Endothelial, 2 0
paths to the root