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RGD uses the Human Disease Ontology (DO, 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:central nervous system mesenchymal non-meningothelial tumor
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Accession:DOID:502 term browser browse the term
Definition:A central nervous system cancer that is characterized by mesenchymal tumors within the CNS that develops from meninges, has_material_basis_in abnormally proliferating cells derives_from mesoderm. (DO)
Synonyms:exact_synonym: Non-meningothelial mesenchymal tumour;   central nervous system mesenchymal non-meningothelial tumour;   non-meningothelial mesenchymal tumor
 primary_id: RDO:9003937
For additional species annotation, visit the Alliance of Genome Resources.

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Term paths to the root
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Term Annotations click to browse term
  disease 16023
    disease of cellular proliferation 5918
      cancer 4242
        organ system cancer 4067
          nervous system cancer 1605
            central nervous system cancer 1288
              central nervous system mesenchymal non-meningothelial tumor 0
                central nervous system chondroma 0
                central nervous system leiomyosarcoma 0
                central nervous system osteosarcoma 0
                ectomesenchymoma 0
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.