JSON

chordoma

^ http://purl.obolibrary.org/obo/MONDO_0008978

Chordomas are rare malignant tumors arising from embryonic remnants of the notochord in axial skeleton. [ Orphanet:178 ]

Term info

database cross reference
  • ICDO:9370/3 (NCIT:C2947)
  • GARD:0001303 (MONDO:equivalentTo)
  • ONCOTREE:CHDM (MONDO:equivalentTo)
  • HP:0010762 (MONDO:otherHierarchy)
  • UMLS:C0008487 (Orphanet:178/e)
  • NCIT:C2947 (MONDO:equivalentTo)
  • MESH:D002817 (Orphanet:178/e)
  • Orphanet:178 (OMIM:215400)
  • MedDRA:10008747 (Orphanet:178/e)
  • OMIM:215400 (Orphanet:178/e)
  • DOID:3302 (MONDO:equivalentTo)
Subsets

ordo_disease

abbreviation
CHDM [ MONDO:Lexical OMIM:215400 ]

IAO 0000589

chordoma (disease)

closeMatch

http://identifiers.org/meddra/10008747

definition

Chordomas are rare malignant tumors arising from embryonic remnants of the notochord in axial skeleton.

exactMatch

http://purl.obolibrary.org/obo/NCIT_C2947, http://purl.obolibrary.org/obo/Orphanet_178, http://purl.obolibrary.org/obo/DOID_3302, http://identifiers.org/mesh/D002817, http://linkedlifedata.com/resource/umls/id/C0008487, https://omim.org/entry/215400

excluded subClassOf

http://purl.obolibrary.org/obo/MONDO_0019833, http://purl.obolibrary.org/obo/MONDO_0015959

has exact synonym

chordoma (disease), notochordal sarcoma, chordoma, notochordoma, chordoma, malignant

has related synonym

CHDM, susceptibility to chordoma, chordoma, susceptibility to

id

MONDO:0008978

Term relations

Subclass of: