t(11;17)(q13;q21)

Preferred Label : t(11;17)(q13;q21);

NCIt synonyms : t 11 17 q13 q21;

Origin ID

C36364;

UMLS CUI

C1515706;

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
- NUMA1/RARA Fusion Gene [NCIt concept]
molecular_abnormality_involves_gene
- NUMA1 Gene [NCIt concept]
- NUMA1/RARA Fusion Gene [NCIt concept]
- RARA Gene [NCIt concept]