{"code":"C20195","name":"Gene Fusion","terminology":"ncit","version":"26.09d","conceptStatus":"DEFAULT","leaf":true,"active":true,"synonyms":[{"name":"Rearrangement Fusion","termType":"SY","type":"FULL_SYN","typeCode":"P90","source":"caDSR"},{"name":"Fusion","termType":"PT","type":"FULL_SYN","typeCode":"P90","source":"CTDC","code":"PV"},{"name":"gene fusion variant","termType":"SY","type":"FULL_SYN","typeCode":"P90","source":"CTDC"},{"name":"gene_fusion_variant","termType":"PT","type":"FULL_SYN","typeCode":"P90","source":"CTDC"},{"name":"Gene Fusion","termType":"PT","type":"FULL_SYN","typeCode":"P90","source":"NCI"},{"name":"Gene Fusion","type":"Preferred_Name","typeCode":"P108"}],"definitions":[{"definition":"Any hybrid gene formed from two previously separate genes. Such fusions occur as a result of translocation, intersititial deletion or chromosomal inversion, and often result in gene products with functions different from the two fusion partners. Gene fusions are associated frequently with hematological cancers, sarcomas and prostate cancer.","code":"P97","type":"DEFINITION","source":"NCI"}],"properties":[{"code":"P322","type":"Contributing_Source","value":"CTDC"},{"code":"P366","type":"Legacy Concept Name","value":"Gene_Fusion"},{"code":"P208","type":"NCI_META_CUI","value":"CL448503"},{"code":"P106","type":"Semantic_Type","value":"Cell or Molecular Dysfunction"}]}