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infant-type hemispheric glioma - Ontology Report - Rat Genome Database

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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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Path 1
Term Annotations click to browse term
  disease 15628
    disease of cellular proliferation 7378
      Neoplasms by Histologic Type 5065
        cell type cancer 3587
          high grade glioma 621
            malignant astrocytoma 444
              infant-type hemispheric glioma 1
Path 2
Term Annotations click to browse term
  disease 15628
    disease of anatomical entity 15289
      nervous system disease 13411
        Nervous System Neoplasms 1506
          Central Nervous System Neoplasms 1336
            central nervous system cancer 689
              brain cancer 674
                supratentorial cancer 477
                  cerebrum cancer 448
                    malignant astrocytoma 444
                      infant-type hemispheric glioma 1
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