Polysomy 17 - CISMeF

Preferred Label : Polysomy 17;

NCIt definition : A chromosomal abnormality characterized by the presence of more than two copies of chromosome 17 in a cell.;

Details

Origin ID

C36657;

UMLS CUI

C1514214;

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
- Breast Ductal Carcinoma In Situ [NCIt concept]
- Breast Ductal Carcinoma In Situ, Comedo Type [NCIt concept]
- Breast Ductal Carcinoma In Situ, Cribriform Pattern [NCIt concept]
- Breast Ductal Carcinoma In Situ, High Grade [NCIt concept]
- Breast Ductal Carcinoma In Situ, Intermediate Grade [NCIt concept]
- Breast Ductal Carcinoma In Situ, Low Grade [NCIt concept]
- Breast Ductal Carcinoma In Situ, Non-Comedo Type [NCIt concept]
- Breast Ductal Carcinoma In Situ, Solid Type [NCIt concept]
- Breast Micropapillary Ductal Carcinoma In Situ [NCIt concept]
- Breast Papillary Ductal Carcinoma In Situ [NCIt concept]
- Breast Solid Papillary Carcinoma In Situ [NCIt concept]
- Recurrent Breast Ductal Carcinoma In Situ [NCIt concept]

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