| Preferred Name |
Chordoma |
| ID |
http://www.orpha.net/ORDO/Orphanet_178 |
| alternative_term |
Notochordal sarcoma |
| definition |
Chordomas are rare malignant tumors arising from embryonic remnants of the notochord in axial skeleton. |
| definition_citation |
Orphanet |
| expertlink |
https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=178 |
| has_age_of_onset |
Adult |
| has_inheritance |
Not applicable Autosomal dominant |
| hasDbXref |
UMLS:C0008487 MeSH:D002817 OMIM:215400 ICD-11:2B5J MedDRA:10008747 ICD-10:C76.7 |
| label |
Chordoma |
| notation |
ORPHA:178 |
| part_of |
http://www.orpha.net/ORDO/Orphanet_100101 http://www.orpha.net/ORDO/Orphanet_271847 http://www.orpha.net/ORDO/Orphanet_68411 |
| prefixIRI |
ORDO:Orphanet_178 |
| prefLabel |
Chordoma |
| present_in |
United States AND has_annual_incidence_average_value : 0.06 AND has_annual_incidence_range : <1 / 1 000 000 |
| treeView |
http://www.orpha.net/ORDO/Orphanet_100101 http://www.orpha.net/ORDO/Orphanet_271847 http://www.orpha.net/ORDO/Orphanet_68411 |
| subClassOf |