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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:Cerebrooculofacioskeletal Syndrome 3
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Accession:DOID:9001554 term browser browse the term
Synonyms:exact_synonym: COFS3
 primary_id: MESH:C565035
 alt_id: OMIM:616570;   RDO:0013789
For additional species annotation, visit the Alliance of Genome Resources.


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Cerebrooculofacioskeletal Syndrome 3 term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G ERCC5 ERCC excision repair 5, endonuclease ISO OMIM NCBI chr13:84,005,950...84,036,710 JBrowse link

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 12749
    syndrome 6164
      Cockayne syndrome 12
        Cerebrooculofacioskeletal Syndrome 5
          Cerebrooculofacioskeletal Syndrome 3 1
Path 2
Term Annotations click to browse term
  disease 12749
    disease of anatomical entity 12279
      musculoskeletal system disease 5158
        connective tissue disease 3581
          bone disease 3083
            bone development disease 1294
              Dwarfism 476
                Cockayne syndrome 12
                  Cerebrooculofacioskeletal Syndrome 5
                    Cerebrooculofacioskeletal Syndrome 3 1
paths to the root

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.