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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:infant-type hemispheric glioma
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Accession:DOID:0081278 term browser browse the term
Definition:A malignant astrocytoma that is characterized by receptor tyrosine kinase fusions in the NTRK family, ROS1, ALK, or MET genes, that arises in the cerebral hemisphere and occurs in early childhood. (DO)
Synonyms:xref: NCI:C185471

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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15274
    disease of cellular proliferation 7181
      Neoplasms by Histologic Type 5034
        cell type cancer 3619
          high grade glioma 684
            malignant astrocytoma 442
              infant-type hemispheric glioma 1
Path 2
Term Annotations click to browse term
  disease 15274
    disease of anatomical entity 14909
      nervous system disease 13001
        Nervous System Neoplasms 1552
          Central Nervous System Neoplasms 1386
            central nervous system cancer 751
              brain cancer 738
                supratentorial cancer 475
                  cerebrum cancer 446
                    malignant astrocytoma 442
                      infant-type hemispheric glioma 1
paths to the root