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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:anaplastic oligodendroglioma
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Accession:DOID:7154 term browser browse the term
Definition:An oligodendroglioma that is characterized by focal or diffuse malignant morphologic features (prominent nuclear pleomorphism, mitoses, and increased cellularity). (DO)
Synonyms:exact_synonym: anaplastic oligodendrogliomas
 xref: EFO:0002501;   NCI:C4326
For additional species annotation, visit the Alliance of Genome Resources.



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anaplastic oligodendroglioma term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G CIC capicua transcriptional repressor ISO ClinVar Annotator: match by term: Anaplastic oligodendroglioma ClinVar NCBI chr19:39,156,204...39,183,498
Ensembl chr19:47,751,520...47,774,699
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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 17996
    disease of cellular proliferation 7241
      cancer 5237
        cell type cancer 3593
          high grade glioma 660
            oligodendroglioma 13
              anaplastic oligodendroglioma 1
                IDH-mutant and 1p/19q-codeleted oligodendroglioma + 0
Path 2
Term Annotations click to browse term
  disease 17996
    disease of anatomical entity 15264
      nervous system disease 13298
        central nervous system disease 11928
          Central Nervous System Neoplasms 1386
            Brain Neoplasms 1339
              brain cancer 715
                high grade glioma 660
                  oligodendroglioma 13
                    anaplastic oligodendroglioma 1
                      IDH-mutant and 1p/19q-codeleted oligodendroglioma + 0
paths to the root