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ONTOLOGY REPORT - ANNOTATIONS


Term:Rett Syndrome, Zappella Variant
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Accession:DOID:9004536 term browser browse the term
Synonyms:primary_id: MESH:C567442;   RDO:0015509
For additional species annotation, visit the Alliance of Genome Resources.


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Rett Syndrome, Zappella Variant term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Mecp2 methyl CpG binding protein 2 JBrowse link X 156,650,389 156,713,813 RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15626
    syndrome 5163
      Rett syndrome 18
        Rett Syndrome, Zappella Variant 1
Path 2
Term Annotations click to browse term
  disease 15626
    disease of anatomical entity 14956
      nervous system disease 10224
        central nervous system disease 8102
          brain disease 7571
            disease of mental health 5520
              developmental disorder of mental health 2712
                specific developmental disorder 1884
                  intellectual disability 1706
                    syndromic intellectual disability 674
                      Mental Retardation, X-Linked 656
                        Rett syndrome 18
                          Rett Syndrome, Zappella Variant 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.