chordoma
notochordal cancer that derives from cellular remnants of the notochord
Facts
8 properties
🏷️ Also known as
en Notochordal sarcoma
en notochordoma
en susceptibility to chordoma
en CHDM
en chordoma
en CHORDOMA, MALIGNANT
en CHORDOMA, SUSCEPTIBILITY TO
en CHORDOMA, SUSCEPTIBILITY TO; CHDM
ar الورم الحبلي
ar ورم حبلي
de Chordom
es Cordoma
fr chordome
ko 척색종
pl Chordoma
pl Struniak
ru Хордома
zh 脊索瘤
🔖 Identifiers · 28
- OpenAlex ID
- C2781190729
- Image (Wikimedia Commons)
- Chordoma.JPG ↗
- Disease Ontology ID
- DOID:3302
- DiseasesDB
- 31483
- EMedicine ID
- 1.3M (251k–1.3M, n=3)
- Encyclopedia of China (Third Edition) ID (2026)
- Ndyr0
- Encyclopedia of China (Third Edition) old ID (2021)
- 464421
- Exact match
- purl.obolibrary.org, identifiers.org, purl.obolibrary.org, www.orpha.net
- Freebase ID
- /m/025tg67
- GARD rare disease ID
- 1303
- Genetics Home Reference Conditions ID
- chordoma
- Human Phenotype Ontology ID
- HP:0010762
Show all 28 identifiers +16
- ICD-10-CM
- C76.7
- ICD-11 ID (Foundation)
- 1455398050
- ICD-11 ID (MMS)
- XH9GH0
- ICD-O
- 9370/3
- JSTOR topic ID (archived)
- chordoma
- MeSH descriptor ID
- D002817
- MeSH tree code
- C04.557.465.220
- Microsoft Academic ID (discontinued)
- 2781190729
- Mondo ID
- MONDO_0008978
- OMIM ID
- 215400
- Orphanet ID
- 178
- PatientsLikeMe condition ID
- chordoma
- Raras disease ID
- D00178
- UMLS CUI
- C0008487
- UniProt disease ID
- DI-02579
🔗 Connections
Genetic association 1
Health specialty 1
On focus list of Wikimedia project 1
Subclass of 1
← Genetic association 1
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