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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 2
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Accession:DOID:9008568 term browser browse the term
Synonyms:exact_synonym: camptodactyly syndrome, Guadalajara type II
 primary_id: MESH:C537971
 alt_id: OMIM:211920
 xref: GARD:1068


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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 17996
    syndrome 10166
      Camptodactyly Syndrome Guadalajara Type 0
        Camptodactyly Syndrome Guadalajara Type 2 0
Path 2
Term Annotations click to browse term
  disease 17996
    Developmental Disease 17885
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 17802
        Congenital Abnormalities 7497
          Musculoskeletal Abnormalities 3270
            Congenital Limb Deformities 1028
              Congenital Upper Extremity Deformities 214
                Congenital Hand Deformities 188
                  Camptodactyly Syndrome Guadalajara Type 0
                    Camptodactyly Syndrome Guadalajara Type 2 0
paths to the root