t(X;1)(p11.2;q21)

Preferred Label : t(X;1)(p11.2;q21);

NCIt synonyms : t X 1 p11 q21;

Origin ID

C37873;

UMLS CUI

C1515816;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 1 [NCIt concept]
- Human Chromosome X [NCIt concept]
is_abnormality_of_gene
- PRCC/TFE3 Fusion Gene [NCIt concept]
- TFE3/PRCC Fusion Gene [NCIt concept]
molecular_abnormality_involves_gene
- PRCC Gene [NCIt concept]
- PRCC/TFE3 Fusion Gene [NCIt concept]
- TFE3 Gene [NCIt concept]
- TFE3/PRCC Fusion Gene [NCIt concept]