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ONTOLOGY REPORT - ANNOTATIONS


Term:retinitis pigmentosa 19
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Accession:DOID:0110354 term browser browse the term
Definition:A retinitis pigmentosa that has_material_basis_in mutation in the ABCA4 gene on chromosome 1p22. (DO)
Synonyms:exact_synonym: RP19
 primary_id: MESH:C566637
 alt_id: OMIM:601718;   RDO:0014943
For additional species annotation, visit the Alliance of Genome Resources.


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retinitis pigmentosa 19 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Abca4 ATP binding cassette subfamily A member 4 JBrowse link 2 225,645,539 225,783,288 RGD:7240710
RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15625
    sensory system disease 4684
      eye and adnexa disease 2252
        eye disease 2252
          Hereditary Eye Diseases 504
            retinitis pigmentosa 239
              retinitis pigmentosa 19 1
Path 2
Term Annotations click to browse term
  disease 15625
    disease of anatomical entity 14954
      nervous system disease 10224
        sensory system disease 4684
          eye and adnexa disease 2252
            eye disease 2252
              retinal disease 715
                retinal degeneration 406
                  fundus dystrophy 263
                    retinitis pigmentosa 239
                      retinitis pigmentosa 19 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.