A slow-growing malignant bone tumor arising from the remnants of the notochord and occurring in the clivus. It is characterized by a lobulated growth pattern, myxoid stroma formation, and the presence of physaliphorous cells. [ NCIT:P378 ]
Synonyms: chordoma (disease) of clivus of occipital bone chordoma of the clivus clivus of occipital bone chordoma (disease) clival chordoma chordoma of clivus
Term information
- DOID:6312 (MONDO:equivalentTo)
- MEDGEN:232372 (MONDO:equivalentTo)
- SCTID:446939001 (MONDO:equivalentTo)
- NCIT:C5412 (MONDO:equivalentTo)
- ICD9:170.0 (MONDO:relatedTo)
- UMLS:C1333071 (MONDO:equivalentTo)
gard_rare, matrix_llm__is_cancer_other, matrix_txgnn_grouping_cancer_or_benign_tumor, harrisons_view_connective_tissue_disorder, matrix_llm__is_glucose_dysfunction_other, matrix_excluded, matrix_llm__tag_qualy_lost_other, mondo_top_grouping_member, matrix_llm__txgnn_other, matrix_llm__medical_specialization_other, mondo_top_grouping_musculoskeletal_system_disorder, 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, harrisons_view_musculoskeletal_system_disorder, mondo_top_grouping_connective_tissue_disorder
http://purl.obolibrary.org/obo/NCIT_C5412
http://linkedlifedata.com/resource/umls/id/C1333071
http://identifiers.org/medgen/232372
http://purl.obolibrary.org/obo/DOID_6312
http://identifiers.org/snomedct/446939001
http://purl.obolibrary.org/obo/mondo/sparql/qc/general/qc-single-child.sparql