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ONTOLOGY REPORT - ANNOTATIONS


Term:Chromosome Xp11.3 Deletion Syndrome
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Accession:DOID:9006850 term browser browse the term
Synonyms:exact_synonym: Mental Retardation, X-Linked, With Retinitis Pigmentosa
 primary_id: MESH:C564481;   RDO:0013427
 alt_id: OMIM:300578
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Chromosome Xp11.3 Deletion Syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Rp2 RP2 activator of ARL3 GTPase JBrowse link X 2,066,298 2,116,661 RGD:7240710

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15489
    syndrome 5228
      Chromosome Xp11.3 Deletion Syndrome 1
Path 2
Term Annotations click to browse term
  disease 15489
    disease of anatomical entity 14790
      nervous system disease 10147
        central nervous system disease 8254
          brain disease 7600
            disease of mental health 5554
              developmental disorder of mental health 2729
                specific developmental disorder 1895
                  intellectual disability 1720
                    syndromic intellectual disability 676
                      Mental Retardation, X-Linked 657
                        Chromosome Xp11.3 Deletion Syndrome 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.