DOID:0081285

• Ontology
• Class
  • owl:Thing
    • host health status
      • disease
        • additional diseases by category
          • disease of anatomical entity
            • nervous system disease
              • central nervous system disease
                • central nervous system benign neoplasm
                  • myxoid glioneuronal tumor
              • nervous system benign neoplasm
                • central nervous system benign neoplasm
                  • myxoid glioneuronal tumor
        • neoplasm
          • benign neoplasm
            • organ system benign neoplasm
              • nervous system benign neoplasm
                • central nervous system benign neoplasm
                  • myxoid glioneuronal tumor
• Annotation Property
• Data Property
• Object Property
• Individual
• Datatype

• label
  • myxoid glioneuronal tumor ^@en
• definition
  • A central nervous system benign neoplasm that is characterized by a dinucleotide mutation at codon 385 of the PDGFR gene. It usually occurs in the septum pellucidum but has also been described in the corpus callosum and periventricular white matter of the lateral ventricle. It is composed of oligodendrocyte-like cells in a prominent myxoid stroma. ^xsd:string
    • oio:hasDbXref
      • url:https://pubmed.ncbi.nlm.nih.gov/34297434/ ^xsd:string
• has exact synonym
  • Myxoid glioneuronal tumour ^xsd:string
• has_obo_namespace
  • disease_ontology ^xsd:string
• id
  • DOID:0081285 ^xsd:string
• in_subset
  • obo:doid#DO_cancer_slim
• oio:hasDbXref
  • ICDO:9509/1 ^xsd:string
  • NCI:C179229 ^xsd:string
• rdf:type
  • owl:Class
• rdfs:subClassOf
  • central nervous system benign neoplasm