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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:retinitis pigmentosa 40
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Accession:DOID:0110375 term browser browse the term
Definition:A retinitis pigmentosa that has_material_basis_in mutation in the PDE6B gene on chromosome 4p16. (DO)
Synonyms:exact_synonym: RP40;   Rod-cone dysplasia 1;   Rod-cone dysplasia 1a
 broad_synonym: PDE6B-RELATED DISORDER
 primary_id: OMIM:613801
 alt_id: OMIA:000882;   OMIA:001669;   RDO:9000498
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 18032
    sensory system disease 6469
      eye disease 3172
        fundus dystrophy 385
          retinitis pigmentosa 310
            retinitis pigmentosa 40 1
Path 2
Term Annotations click to browse term
  disease 18032
    disease of anatomical entity 17412
      nervous system disease 13079
        sensory system disease 6469
          eye disease 3172
            retinal disease 865
              retinal degeneration 525
                fundus dystrophy 385
                  retinitis pigmentosa 310
                    retinitis pigmentosa 40 1
paths to the root