Monosomy 16 - CISMeF

Preferred Label : Monosomy 16;

NCIt definition : A chromosomal abnormality characterized by the absence of one of the copies of chromosome 16.;

Details

Origin ID

C36384;

UMLS CUI

C1513479;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 16 [NCIt concept]
may_be_cytogenetic_abnormality_of_disease
- Pleomorphic Lipoma [NCIt concept]
- Skin Pleomorphic Lipoma [NCIt concept]
- Skin Spindle Cell Lipoma [NCIt concept]
- Skin Spindle Cell/Pleomorphic Lipoma [NCIt concept]
- Spindle Cell Lipoma [NCIt concept]
- Spindle Cell/Pleomorphic Lipoma [NCIt concept]
- Sporadic Breast Carcinoma [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