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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:Xeroderma Pigmentosum B / Cockayne Syndrome
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Accession:DOID:9006765 term browser browse the term
Synonyms:primary_id: MESH:C567061
 alt_id: RDO:0015239
For additional species annotation, visit the Alliance of Genome Resources.

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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 17774
    syndrome 7565
      Cockayne syndrome 15
        Xeroderma Pigmentosum B / Cockayne Syndrome 0
Path 2
Term Annotations click to browse term
  disease 17774
    disease of anatomical entity 16335
      nervous system disease 12618
        sensory system disease 5474
          skin disease 2832
            dermatitis 383
              photosensitivity disease 31
                xeroderma pigmentosum 20
                  xeroderma pigmentosum group B 1
                    Xeroderma Pigmentosum B / Cockayne Syndrome 0
paths to the root


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.