C165248Level 5

t(17;19)

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A cytogenetic abnormality that involves a translocation between chromosomes 17 and 19.

GET/api/v1/systems/nci_thesaurus/nodes/C165248

Official DownloadCC BY 4.0Source

Hierarchy Explorer

No cross-system equivalences mapped for this node.