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ONTOLOGY REPORT - ANNOTATIONS


Term:Retinal Dysplasia
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Accession:DOID:9006597 term browser browse the term
Definition:Congenital, often bilateral, retinal abnormality characterized by the arrangement of outer nuclear retinal cells in a palisading or radiating pattern surrounding a central ocular space. This disorder is sometimes hereditary.
Synonyms:exact_synonym: Retinal Dysplasias
 primary_id: MESH:D015792;   RDO:0003599
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Retinal Dysplasia term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Crb1 crumbs cell polarity complex component 1 JBrowse link 13 56,270,519 56,462,893 RGD:8552698
G Slbp stem-loop binding protein JBrowse link 14 82,356,916 82,366,368 RGD:11554173
microcephaly with or without chorioretinopathy, lymphedema, or mental retardation term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Kif11 kinesin family member 11 JBrowse link 1 256,035,866 256,088,299 RGD:7240710
RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15639
    sensory system disease 4697
      eye and adnexa disease 2257
        eye disease 2257
          retinal disease 715
            Retinal Dysplasia 3
              Primary Retinal Dysplasia 0
              Reese Retinal Dysplasia 0
              microcephaly with or without chorioretinopathy, lymphedema, or mental retardation 1
Path 2
Term Annotations click to browse term
  disease 15639
    disease of anatomical entity 14969
      nervous system disease 10242
        sensory system disease 4697
          eye and adnexa disease 2257
            eye disease 2257
              Hereditary Eye Diseases 505
                Retinal Dysplasia 3
                  Primary Retinal Dysplasia 0
                  Reese Retinal Dysplasia 0
                  microcephaly with or without chorioretinopathy, lymphedema, or mental retardation 1
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.