Monosomy 6 - CISMeF

Preferred Label : Monosomy 6;

NCIt definition : A chromosomal abnormality consisting of the absence of one complete copy of chromosome 6 in somatic cells.;

Details

Origin ID

C36627;

UMLS CUI

C1513482;

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 6 [NCIt concept]
may_be_cytogenetic_abnormality_of_disease
- Posterior Fossa Ependymoma, Group B (PFB) [NCIt concept]
- Sporadic Breast Carcinoma [NCIt concept]

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