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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 Habitus, Osteopenia, and Camptodactyly
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Accession:DOID:9005814 term browser browse the term
Synonyms:exact_synonym: Urban Rogers Meyer syndrome
 primary_id: MESH:C538276
 alt_id: OMIM:264010

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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 16063
    syndrome 9327
      Prader-Willi syndrome 16
        Prader-Willi Habitus, Osteopenia, and Camptodactyly 0
Path 2
Term Annotations click to browse term
  disease 16063
    disease of anatomical entity 13820
      nervous system disease 12088
        central nervous system disease 10855
          brain disease 10186
            disease of mental health 7327
              developmental disorder of mental health 4976
                specific developmental disorder 4103
                  intellectual disability 3919
                    Prader-Willi syndrome 16
                      Prader-Willi Habitus, Osteopenia, and Camptodactyly 0
paths to the root