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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:Familial Synovial Chondromatosis with Dwarfism
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Accession:DOID:9003213 term browser browse the term
Synonyms:primary_id: MESH:C566087
 alt_id: OMIM:186575


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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 18976
    disease of anatomical entity 18260
      endocrine system disease 6819
        Dwarfism 865
          Familial Synovial Chondromatosis with Dwarfism 0
Path 2
Term Annotations click to browse term
  disease 18976
    disease of anatomical entity 18260
      musculoskeletal system disease 8304
        connective tissue disease 5786
          bone disease 4302
            bone inflammation disease 1494
              arthropathy 1473
                Synovial Chondromatosis 0
                  Familial Synovial Chondromatosis with Dwarfism 0
paths to the root