C36622Level 5
del(8p12-p21)
**Semantic type:** Cell or Molecular Dysfunction
**Definition:** A cytogenetic abnormality characterized by any loss of genetic material from the short arm of chromosome 8 within the 8p12-p21 region.
**Synonyms:** - del(8)(p12p21) - del(8p12p21)
GET
/api/v1/systems/nci_thesaurus/nodes/C36622Hierarchy Explorer
Loading...
Cross-system equivalences0
No cross-system equivalences mapped for this node.