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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 LOC101968680 DNA repair protein complementing XP-G cells ISO OMIM NCBI chrNW_004936472:8,209,482...8,234,696 JBrowse link

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 11938
    syndrome 5829
      Cockayne syndrome 12
        Cerebrooculofacioskeletal Syndrome 5
          Cerebrooculofacioskeletal Syndrome 3 1
Path 2
Term Annotations click to browse term
  disease 11938
    disease of anatomical entity 11499
      musculoskeletal system disease 4947
        connective tissue disease 3413
          bone disease 2949
            bone development disease 1258
              Dwarfism 461
                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.