inv(16) - CISMeF

Preferred Label : inv(16);

NCIt definition : A chromosomal inversion that involves chromosome 16.;

Origin ID

C119609;

UMLS CUI

C3897144;

Automatic exact mappings (from CISMeF team)
- inv (16) [EMDN type]
- inv (16) [medical devices type]
Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
concept_is_in_subset
- CPTAC Acute Myeloid Leukemia Baseline Form [NCIt concept]
- CPTAC Baseline Medical Forms Terminology [NCIt concept]
- CPTAC Terminology [NCIt concept]
- CTRP Biomarker Terminology [NCIt concept]
- CTRP Molecular Genetic Biomarker Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 16 [NCIt concept]