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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:Camptodactyly Syndrome Guadalajara Type
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Accession:DOID:9008935 term browser browse the term


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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 17773
    syndrome 10064
      Camptodactyly Syndrome Guadalajara Type 0
        Camptodactyly Syndrome Guadalajara Type 1 0
        Camptodactyly Syndrome Guadalajara Type 2 0
        Camptodactyly Syndrome Guadalajara Type 3 0
Path 2
Term Annotations click to browse term
  disease 17773
    Developmental Disease 17564
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 17452
        Congenital Abnormalities 7452
          Musculoskeletal Abnormalities 3260
            Congenital Limb Deformities 1017
              Congenital Upper Extremity Deformities 215
                Congenital Hand Deformities 187
                  Camptodactyly Syndrome Guadalajara Type 0
                    Camptodactyly Syndrome Guadalajara Type 1 0
                    Camptodactyly Syndrome Guadalajara Type 2 0
                    Camptodactyly Syndrome Guadalajara Type 3 0
paths to the root