A benign or malignant brain and spinal cord tumor that arises from glial cells (astrocytes, oligodendrocytes, ependymal cells). Tumors that arise from astrocytes are called astrocytic tumors or astrocytomas. Tumors that arise from oligodendrocytes are called oligodendroglial tumors. Tumors that arise from ependymal cells are called ependymomas. [ NCIT:C3059 ]

Synonyms: tumor of neuroglia glial tumor tumor of the neuroglia neuroglial tumour glial tumour tumour of neuroglia neuroglial tumor glial neoplasm tumour of the neuroglia glioma neoplasm of the neuroglia neoplasm of neuroglia neuroglial neoplasm

This is just here as a test because I lose it

Term information

database cross reference
  • UMLS:C0017638 (MONDO:equivalentTo)
  • Orphanet:182067 (https://github.com/monarch-initiative/mondo/issues/2932)
  • EFO:0005543 (MONDO:equivalentTo)
  • MESH:D005910 (MONDO:equivalentTo)
  • NCIT:C3059 (MONDO:equivalentTo)
  • SCTID:393564001 (MONDO:equivalentTo)
  • GARD:6513 (MONDO:GARD)
  • MEDGEN:9030 (MONDO:equivalentTo)
Subsets

gard_rare, matrix_llm__is_cancer_other, matrix_txgnn_grouping_cancer_or_benign_tumor, matrix_llm__is_glucose_dysfunction_other, matrix_excluded, otar, matrix_llm__tag_qualy_lost_other, mondo_top_grouping_member, matrix_llm__txgnn_other, matrix_llm__medical_specialization_other, matrix_llm__tag_existing_treatment_other, nord_rare, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, mondo_top_grouping_cancer_or_benign_tumor, matrix_txgnn_grouping_member, harrisons_view_cancer_or_benign_tumor, rare, harrisons_view_member, mondo_top_grouping_nervous_system_disorder, harrisons_view_nervous_system_disorder, ordo_group_of_disorders

UK spelling synonym
glial tumour

UK spelling synonym
neuroglial tumour

UK spelling synonym
tumour of the neuroglia

UK spelling synonym
tumour of neuroglia

exactMatch

http://identifiers.org/mesh/D005910

http://purl.obolibrary.org/obo/NCIT_C3059

http://linkedlifedata.com/resource/umls/id/C0017638

http://www.ebi.ac.uk/efo/EFO_0005543

http://identifiers.org/medgen/9030

http://identifiers.org/snomedct/393564001

http://www.orpha.net/ORDO/Orphanet_182067

id

MONDO:0021042