Monosomy 17 - CISMeF

Preferred Label : Monosomy 17;

NCIt definition : A chromosomal abnormality consisting of the absence of one of the copies of chromosome 17.;

Origin ID

C36509;

UMLS CUI

C1513480;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
concept_is_in_subset
- CTRP Biomarker Terminology [NCIt concept]
- CTRP Molecular Genetic Biomarker Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 17 [NCIt concept]
may_be_cytogenetic_abnormality_of_disease
- Sporadic Breast Carcinoma [NCIt concept]