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RGD DISEASE ONTOLOGY - ANNOTATIONS

RGD uses the Human Disease Ontology (DO, https://disease-ontology.org/) 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:Prader-Willi-Like Syndrome Associated with Chromosome 6
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Accession:DOID:9003498 term browser browse the term
Synonyms:primary_id: MESH:C566764;   RDO:0015021

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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14197
    syndrome 9389
      Prader-Willi syndrome 16
        Prader-Willi-Like Syndrome Associated with Chromosome 6 0
Path 2
Term Annotations click to browse term
  disease 14197
    disease of anatomical entity 13866
      nervous system disease 12143
        central nervous system disease 10896
          brain disease 10230
            disease of mental health 7352
              developmental disorder of mental health 4992
                specific developmental disorder 4121
                  intellectual disability 3933
                    Prader-Willi syndrome 16
                      Prader-Willi-Like Syndrome Associated with Chromosome 6 0
paths to the root