{"count":43797,"next":"https://cinder.proteo.info/api/ms_vocab/?format=json&limit=20&offset=27480&ordering=-name","previous":"https://cinder.proteo.info/api/ms_vocab/?format=json&limit=20&offset=27440&ordering=-name","results":[{"accession":"CLO:0010691","name":"GM09212 cell","definition":"[' MAJOR AFFECTIVE DISORDER; OLD ORDER AMISH - 125480 OR 309200']","term_type":"cell line"},{"accession":"CLO:0010692","name":"GM09211 cell","definition":"[' MAJOR AFFECTIVE DISORDER; OLD ORDER AMISH - 125480 OR 309200']","term_type":"cell line"},{"accession":"CLO:0010688","name":"GM09210 cell","definition":"[' MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS CHROMOSOME DELETION']","term_type":"cell line"},{"accession":"CLO:0010636","name":"GM09209 cell","definition":"[' MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS CHROMOSOME DELETION']","term_type":"cell line"},{"accession":"CLO:0010635","name":"GM09208 cell","definition":"[' MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS CHROMOSOME DELETION']","term_type":"cell line"},{"accession":"CLO:0010640","name":"GM09197 cell","definition":"[' HUNTINGTON DISEASE; HD']","term_type":"cell line"},{"accession":"CLO:0010639","name":"GM09196 cell","definition":"[' MENKES SYNDROME']","term_type":"cell line"},{"accession":"CLO:0010638","name":"GM09195 cell","definition":"[' MENKES SYNDROME']","term_type":"cell line"},{"accession":"CLO:0010637","name":"GM09194 cell","definition":"[' MENKES SYNDROME']","term_type":"cell line"},{"accession":"CLO:0010634","name":"GM09193 cell","definition":"[' MAJOR AFFECTIVE DISORDER; OLD ORDER AMISH - 125480 OR 309200']","term_type":"cell line"},{"accession":"CLO:0010633","name":"GM09192 cell","definition":"[' TRANSLOCATED CHROMOSOME']","term_type":"cell line"},{"accession":"CLO:0010632","name":"GM09191 cell","definition":"[' CHROMOSOME 6 REGIONAL MAPPING PANEL SOMATIC CELL HYBRIDS ADDITIONAL DELETION/DERIVATIVE X CHROMOSOME SOMATIC CELL HYBRIDS']","term_type":"cell line"},{"accession":"CLO:0010631","name":"GM09189 cell","definition":"[' PRADER-WILLI SYNDROME; PWS CHROMOSOME DELETION']","term_type":"cell line"},{"accession":"CLO:0010624","name":"GM09154 cell","definition":"[' NEUROAXONAL DYSTROPHY, INFANTILE']","term_type":"cell line"},{"accession":"CLO:0010626","name":"GM09153 cell","definition":"[' HEMOGLOBIN--BETA LOCUS; HBB']","term_type":"cell line"},{"accession":"CLO:0010625","name":"GM09146 cell","definition":"[' FRAGILE SITE MENTAL RETARDATION 1; FMR1']","term_type":"cell line"},{"accession":"CLO:0010628","name":"GM09145 cell","definition":"[' FRAGILE SITE MENTAL RETARDATION 1; FMR1']","term_type":"cell line"},{"accession":"CLO:0010627","name":"GM09142 cell","definition":"[' CHROMOSOME 21 REGIONAL MAPPING PANEL SOMATIC CELL HYBRIDS CHROMOSOME X REGIONAL MAPPING PANEL SOMATIC CELL HYBRIDS']","term_type":"cell line"},{"accession":"CLO:0010630","name":"GM09138 cell","definition":"[' MAJOR AFFECTIVE DISORDER; OLD ORDER AMISH - 125480 OR 309200']","term_type":"cell line"},{"accession":"CLO:0010629","name":"GM09133 cell","definition":"[' CHROMOSOME DELETION PRADER-WILLI SYNDROME; PWS']","term_type":"cell line"}]}