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ONTOLOGY REPORT - ANNOTATIONS


Term:bradyopsia
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Accession:DOID:0050335 term browser browse the term
Definition:A retinal disease characterized by the slower than usual adaptation of the eyes to changing light conditions; can have material basis in mutations in the RGS9 or the R9AP genes. (DO)
Synonyms:exact_synonym: PERRS;   prolonged electroretinal response suppression
 primary_id: MESH:C564243;   RDO:0013269
 alt_id: OMIM:608415
 xref: GARD:12299;   ORDO:75374
For additional species annotation, visit the Alliance of Genome Resources.


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bradyopsia term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Rgs9 regulator of G-protein signaling 9 JBrowse link 10 97,509,971 97,582,188 RGD:7240710
RGD:8554872
G Rgs9bp regulator of G protein signaling 9 binding protein JBrowse link 1 91,855,270 91,855,983 RGD:7240710
RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15603
    sensory system disease 4697
      eye and adnexa disease 2259
        eye disease 2259
          retinal disease 715
            bradyopsia 2
Path 2
Term Annotations click to browse term
  disease 15603
    disease of anatomical entity 14934
      nervous system disease 10239
        sensory system disease 4697
          eye and adnexa disease 2259
            eye disease 2259
              Hereditary Eye Diseases 505
                bradyopsia 2
paths to the root

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