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RGD uses the Human Disease Ontology (DO, for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.

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
For additional species annotation, visit the Alliance of Genome Resources.

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Chromosome Xp11.3 Deletion Syndrome term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Rp2 RP2 activator of ARL3 GTPase ISO OMIM NCBI chr  X:2,066,298...2,116,661
Ensembl chr  X:2,064,486...2,116,656
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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 16909
    syndrome 7568
      Chromosome Xp11.3 Deletion Syndrome 1
Path 2
Term Annotations click to browse term
  disease 16909
    disease of anatomical entity 16281
      nervous system disease 11853
        central nervous system disease 10192
          brain disease 9565
            disease of mental health 6921
              developmental disorder of mental health 4267
                specific developmental disorder 3531
                  intellectual disability 3384
                    syndromic intellectual disability 752
                      Mental Retardation, X-Linked 717
                        Chromosome Xp11.3 Deletion Syndrome 1
paths to the root