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:retinitis pigmentosa 29
go back to main search page
Accession:DOID:0110378 term browser browse the term
Definition:A retinitis pigmentosa that has_material_basis_in variation in the chromosome region 4q32-q34. (DO)
Synonyms:exact_synonym: RP29
 primary_id: MESH:C567403
 alt_id: OMIM:612165



show annotations for term's descendants           Sort by:

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 21120
    sensory system disease 6930
      eye disease 3462
        fundus dystrophy 699
          retinitis pigmentosa 603
            retinitis pigmentosa 29 0
Path 2
Term Annotations click to browse term
  disease 21120
    disease of anatomical entity 18195
      nervous system disease 14031
        Neurologic Manifestations 10017
          sensory system disease 6930
            eye disease 3462
              eye degenerative disease 848
                retinal degeneration 846
                  fundus dystrophy 699
                    retinitis pigmentosa 603
                      retinitis pigmentosa 29 0
paths to the root