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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:retinitis pigmentosa 4
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Accession:DOID:0110372 term browser browse the term
Definition:A retinitis pigmentosa that has_material_basis_in mutation in the RHO gene on chromosome 3q22. (DO)
Synonyms:exact_synonym: RP4;   rhodopsin-related retinitis pigmentosa
 narrow_synonym: retinitis pigmentosa 4, autosomal recessive
 primary_id: MESH:C566706
 alt_id: OMIM:613731
For additional species annotation, visit the Alliance of Genome Resources.

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retinitis pigmentosa 4 term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Rho rhodopsin ISO ClinVar Annotator: match by OMIM:613731
ClinVar Annotator: match by term: Retinitis pigmentosa 4, autosomal recessive
PMID:1301135, PMID:1302614, PMID:1303237, PMID:1356370, PMID:1418997, PMID:1484692, PMID:1539595, PMID:1580841, PMID:1765377, PMID:1783387, PMID:1808803, PMID:1833777, PMID:1840561, PMID:1862076, PMID:1882937, PMID:1897520, PMID:1924344, PMID:1929926, PMID:1985460, PMID:1987955, PMID:1987956, PMID:2137202, PMID:2215617, PMID:2239971, PMID:2333895, PMID:2613244, PMID:7523628, PMID:7987331, PMID:7987385, PMID:8045708, PMID:8088850, PMID:8240107, PMID:8253795, PMID:8317502, PMID:8328469, PMID:8353500, PMID:8401533, PMID:8406457, PMID:8554077, PMID:8841304, PMID:8905849, PMID:8943080, PMID:9197578, PMID:9483582, PMID:9724753, PMID:9810568, PMID:10967073, PMID:10980774, PMID:11094174, PMID:11139241, PMID:11879142, PMID:11910130, PMID:12091393, PMID:12660238, PMID:14769795, PMID:15509574, PMID:16737970, PMID:17488458, PMID:18175313, PMID:19085385, PMID:19913029, PMID:19960070, PMID:20555336, PMID:21094163, PMID:21174529, PMID:21352497, PMID:22252712, PMID:22323724, PMID:23221340, PMID:23591405, PMID:23625926, PMID:24265693, PMID:24520188, PMID:24853414, PMID:24935155, PMID:24938718, PMID:25096327, PMID:25101269, PMID:25221422, PMID:25408095, PMID:25741868, PMID:25741869, PMID:26887858, PMID:27624628, PMID:28041643, PMID:28076437, PMID:28492532, PMID:28559085, PMID:28981474, PMID:29068140, PMID:29847639, PMID:30240733, PMID:30311386, PMID:30718709, PMID:31100078 NCBI chr 4:147,832,136...147,837,298
Ensembl chr 4:147,832,136...147,837,298
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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 16023
    sensory system disease 5231
      eye disease 2664
        Hereditary Eye Diseases 580
          retinitis pigmentosa 270
            retinitis pigmentosa 4 1
Path 2
Term Annotations click to browse term
  disease 16023
    disease of anatomical entity 15278
      nervous system disease 10897
        sensory system disease 5231
          eye disease 2664
            retinal disease 783
              retinal degeneration 468
                fundus dystrophy 339
                  retinitis pigmentosa 270
                    retinitis pigmentosa 4 1
paths to the root


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