{"code":"C99752","name":"Indel Mutation","terminology":"ncit","version":"26.09d","conceptStatus":"DEFAULT","leaf":false,"active":true,"synonyms":[{"name":"indel variant","termType":"SY","type":"FULL_SYN","typeCode":"P90","source":"CTDC"},{"name":"indel_variant","termType":"PT","type":"FULL_SYN","typeCode":"P90","source":"CTDC"},{"name":"INDEL","termType":"PT","type":"FULL_SYN","typeCode":"P90","source":"FDA","subSource":"pFDA"},{"name":"Indel","termType":"SY","type":"FULL_SYN","typeCode":"P90","source":"NCI"},{"name":"Indel Mutation","termType":"PT","type":"FULL_SYN","typeCode":"P90","source":"NCI"},{"name":"Insertion-Deletion","termType":"SY","type":"FULL_SYN","typeCode":"P90","source":"NCI"},{"name":"Indel Mutation","type":"Preferred_Name","typeCode":"P108"}],"definitions":[{"definition":"A mutation class that includes insertion mutations, deletion mutations and mutation events where both an insertion and a deletion has occurred.","code":"P97","type":"DEFINITION","source":"NCI"}],"properties":[{"code":"P322","type":"Contributing_Source","value":"CTDC"},{"code":"P322","type":"Contributing_Source","value":"FDA"},{"code":"P106","type":"Semantic_Type","value":"Cell or Molecular Dysfunction"},{"code":"P207","type":"UMLS_CUI","value":"C1956002"}]}