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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 17472
    sensory system disease 6502
      eye disease 3328
        corneal disease 219
          corneal dystrophy 51
            corneal endothelial dystrophy 10
              Fuchs' endothelial dystrophy 9
                Corneal Dystrophy, Fuchs' Endothelial, 2 0
Path 2
Term Annotations click to browse term
  disease 17472
    Pathological Conditions, Signs and Symptoms 11770
      Signs and Symptoms 9735
        Neurologic Manifestations 9411
          sensory system disease 6502
            eye disease 3328
              Hereditary Eye Diseases 1064
                corneal dystrophy 51
                  corneal endothelial dystrophy 10
                    Fuchs' endothelial dystrophy 9
                      Corneal Dystrophy, Fuchs' Endothelial, 2 0
paths to the root