Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   

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
go back to main search page
Accession:DOID:9008568 term browser browse the term
Synonyms:exact_synonym: camptodactyly syndrome, Guadalajara type II
 primary_id: MESH:C537971;   MESH:C567138
 alt_id: OMIM:211920
 xref: GARD:1068
For additional species annotation, visit the Alliance of Genome Resources.


show annotations for term's descendants           Sort by:
 

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 16937
    syndrome 7656
      Camptodactyly Syndrome Guadalajara Type 0
        Camptodactyly Syndrome Guadalajara Type 2 0
Path 2
Term Annotations click to browse term
  disease 16937
    Developmental Disease 10589
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 8895
        Congenital Abnormalities 5194
          Musculoskeletal Abnormalities 2135
            Congenital Limb Deformities 453
              Congenital Upper Extremity Deformities 89
                Congenital Hand Deformities 74
                  Camptodactyly Syndrome Guadalajara Type 0
                    Camptodactyly Syndrome Guadalajara Type 2 0
paths to the root