t(11;17)(q23;q21)

Preferred Label : t(11;17)(q23;q21);

NCIt synonyms : t 11 17 q23 q21;

Origin ID

C36363;

UMLS CUI

C1515708;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 11 [NCIt concept]
- Human Chromosome 17 [NCIt concept]
is_abnormality_of_gene
- RARA/ZBTB16 Fusion Gene [NCIt concept]
- ZBTB16/RARA Fusion Gene [NCIt concept]
molecular_abnormality_involves_gene
- RARA Gene [NCIt concept]
- RARA/ZBTB16 Fusion Gene [NCIt concept]
- ZBTB16 Gene [NCIt concept]
- ZBTB16/RARA Fusion Gene [NCIt concept]