Monosomy 3 - CISMeF

Preferred Label : Monosomy 3;

NCIt definition : A chromosomal abnormality consisting of the absence of a copy (homolog) of chromosome 3.;

Origin ID

C43305;

UMLS CUI

C1709071;

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 3 [NCIt concept]
is_cytogenetic_abnormality_of_disease
- Uveal Class 2 Melanoma [NCIt concept]
is_not_cytogenetic_abnormality_of_disease
- Uveal Class 1 Melanoma [NCIt concept]
- Uveal Class 1a Melanoma [NCIt concept]
- Uveal Class 1b Melanoma [NCIt concept]