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chordoma

Disease Summary
Associated Targets (1)
Tbio

1


GARD Rare
Mondo Description Chordomas are rare malignant tumors arising from embryonic remnants of the notochord in axial skeleton.
Uniprot Description Rare, clinically malignant tumors derived from notochordal remnants. They occur along the length of the spinal axis, predominantly in the sphenooccipital, vertebral and sacrococcygeal regions. They are characterized by slow growth, local destruction of bone, extension into adjacent soft tissues and rarely, distant metastatic spread.
Disease Ontology Description A notochordal cancer that derives_from cellular remnants of the notochord.
Mondo Term and Equivalent IDs
MONDO:0008978:  chordoma
GARD:0001303: 
MESH:D002817: 
NCIT:C2947: 
ONCOTREE:CHDM: 
Orphanet:178: 
UMLS:C0008487: