t(15;19)(q13;p13.1)

Preferred Label : t(15;19)(q13;p13.1);

NCIt synonyms : t 15 19 q13 p13 1;

Origin ID

C45717;

UMLS CUI

C1711145;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 15 [NCIt concept]
- Human Chromosome 19 [NCIt concept]
is_cytogenetic_abnormality_of_disease
- Advanced NUT Carcinoma [NCIt concept]
- Childhood Head and Neck NUT Carcinoma [NCIt concept]
- Childhood NUT Carcinoma [NCIt concept]
- Head and Neck NUT Carcinoma [NCIt concept]
- Mediastinal/Thymus NUT Carcinoma [NCIt concept]
- Metastatic NUT Carcinoma [NCIt concept]
- NUT Carcinoma [NCIt concept]
- Primary Cutaneous NUT Adnexal Carcinoma [NCIt concept]
- Sinonasal NUT Carcinoma [NCIt concept]
- Thoracic NUT Carcinoma [NCIt concept]
- Unresectable NUT Carcinoma [NCIt concept]
is_not_cytogenetic_abnormality_of_disease
- Thymus Undifferentiated Carcinoma [NCIt concept]
molecular_abnormality_involves_gene
- BRD4 Gene [NCIt concept]
- BRD4/NUTM1 Fusion Gene [NCIt concept]
- NUTM1 Gene [NCIt concept]