del(1p13-p22) - CISMeF

Preferred Label : del(1p13-p22);

NCIt synonyms : del 1p13-22; del(1p13-22);

NCIt definition : A cytogenetic abnormality characterized by any loss of genetic material from the short arm of chromosome 1 within the 1p13-p22 region.;

Détails

Origin ID

C36570;

UMLS CUI

C1515591;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 1 [NCIt concept]
may_be_cytogenetic_abnormality_of_disease
- Localized Chondrosarcoma [NCIt concept]
- Locally Advanced Chondrosarcoma [NCIt concept]
- Locally Advanced Unresectable Primary Central Chondrosarcoma [NCIt concept]
- Metastatic Chondrosarcoma [NCIt concept]
- Metastatic Primary Central Chondrosarcoma [NCIt concept]
- Primary Central Chondrosarcoma [NCIt concept]
- Recurrent Chondrosarcoma [NCIt concept]
- Unresectable Primary Central Chondrosarcoma [NCIt concept]

Position du mot-clé dans l'(les) arborescence(s) :

Vous pouvez consulter :

recommendations
documents concerning education
documents for patients