Chromosome 17 Abnormality

Preferred Label : Chromosome 17 Abnormality;

NCIt definition : An irregularity in the structure of chromosome 17.;

NCI Metathesaurus CUI : CL512691;

Details

Origin ID

C129438;

UMLS CUI

C4329664;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 17 [NCIt concept]
may_be_cytogenetic_abnormality_of_disease
- Medulloblastoma, Non-WNT/Non-SHH, Group 4 [NCIt concept]

Keyword's position in hierarchy(ies) :

You can consult :

All resources
or only the major
or use the search engine

recommendations
documents concerning education
documents for patients