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RGD uses the Human Disease Ontology (DO, 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:Caudal Duplication Anomaly
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Accession:DOID:9002004 term browser browse the term
Synonyms:primary_id: MESH:C564315;   RDO:0013323
 alt_id: OMIM:607864
For additional species annotation, visit the Alliance of Genome Resources.

show annotations for term's descendants           Sort by:
Caudal Duplication Anomaly term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Axin1 axin 1 ISO OMIM NCBI chr10:15,163,684...15,215,615
Ensembl chr10:15,163,684...15,215,615
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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 17289
    Developmental Disease 10990
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 9530
        Congenital Abnormalities 5603
          Caudal Duplication Anomaly 1
paths to the root