{"code":"C63547","name":"Haplotype","terminology":"ncit","version":"26.09d","conceptStatus":"DEFAULT","leaf":false,"active":true,"synonyms":[{"name":"Haplo","termType":"SY","type":"FULL_SYN","typeCode":"P90","source":"caDSR"},{"name":"HAPLOTYPE","termType":"PT","type":"FULL_SYN","typeCode":"P90","source":"CDISC"},{"name":"haplotype","termType":"PT","type":"FULL_SYN","typeCode":"P90","source":"NCI-GLOSS","code":"CDR0000485392"},{"name":"Haplotype","termType":"PT","type":"FULL_SYN","typeCode":"P90","source":"NCI"},{"name":"Haplotype","type":"Preferred_Name","typeCode":"P108"}],"definitions":[{"definition":"A set of closely linked genetic markers present on one chromosome which tend to be inherited together.","code":"P325","type":"ALT_DEFINITION","source":"NCI-GLOSS"},{"definition":"A way of denoting the collective genotype of a number of closely linked loci on a chromosome.","code":"P97","type":"DEFINITION","source":"NCI"},{"definition":"The combination of linked marker alleles for a given region of DNA on a single chromosome. (Glossary of Genomics Terms. JAMA. 2013 Apr 10; 309(14):1533-35.)","code":"P325","type":"ALT_DEFINITION","source":"CDISC"}],"properties":[{"code":"P322","type":"Contributing_Source","value":"CDISC"},{"code":"P366","type":"Legacy Concept Name","value":"Haplotype"},{"code":"P106","type":"Semantic_Type","value":"Organism Attribute"},{"code":"P207","type":"UMLS_CUI","value":"C0018591"}]}