{"count":43797,"next":"https://cinder.proteo.info/api/ms_vocab/?format=json&limit=20&offset=15180&ordering=name","previous":"https://cinder.proteo.info/api/ms_vocab/?format=json&limit=20&offset=15140&ordering=name","results":[{"accession":"CLO:0023094","name":"GM06228 cell","definition":"[' TRANSLOCATED CHROMOSOME']","term_type":"cell line"},{"accession":"CLO:0023093","name":"GM06229 cell","definition":"[' TRANSLOCATED CHROMOSOME']","term_type":"cell line"},{"accession":"CLO:0023095","name":"GM06230 cell","definition":"[' ANEUPLOID CHROMOSOME NUMBER - TRISOMY']","term_type":"cell line"},{"accession":"CLO:0023106","name":"GM06231 cell","definition":"[' ZELLWEGER SYNDROME; ZS']","term_type":"cell line"},{"accession":"CLO:0023107","name":"GM06246 cell","definition":"[' DICENTRIC CHROMOSOME']","term_type":"cell line"},{"accession":"CLO:0023108","name":"GM06248 cell","definition":"[' ALBUMIN; ALB DYSALBUMINEMIC HYPERTHYROXINEMIA, INCLUDED INVERTED CHROMOSOME']","term_type":"cell line"},{"accession":"CLO:0023109","name":"GM06256 cell","definition":"[' ZELLWEGER SYNDROME; ZS INVERTED CHROMOSOME']","term_type":"cell line"},{"accession":"CLO:0023110","name":"GM06260 cell","definition":"[' OSTEOGENESIS IMPERFECTA: GENETICS UNCERTAIN; LETHAL']","term_type":"cell line"},{"accession":"CLO:0023111","name":"GM06261 cell","definition":"[' EHLERS-DANLOS SYNDROME: TYPE IV; ARTERIAL, ECCHYMOTIC TYPE']","term_type":"cell line"},{"accession":"CLO:0023115","name":"GM06273 cell","definition":"[' HUNTINGTON DISEASE; HD']","term_type":"cell line"},{"accession":"CLO:0023114","name":"GM06274 cell","definition":"[' HUNTINGTON DISEASE; HD']","term_type":"cell line"},{"accession":"CLO:0023113","name":"GM06275 cell","definition":"[' TRANSLOCATED CHROMOSOME']","term_type":"cell line"},{"accession":"CLO:0023112","name":"GM06312 cell","definition":"[' CHROMOSOME DELETION']","term_type":"cell line"},{"accession":"CLO:0023128","name":"GM06314 cell","definition":"[' GLYCOGEN STORAGE DISEASE II GLUCOSIDASE, ALPHA, ACID; GAA']","term_type":"cell line"},{"accession":"CLO:0023126","name":"GM06315 cell","definition":"[' APPARENTLY HEALTHY NON-FETAL TISSUE']","term_type":"cell line"},{"accession":"CLO:0023127","name":"GM06316 cell","definition":"[' TRANSLOCATED CHROMOSOME']","term_type":"cell line"},{"accession":"CLO:0023131","name":"GM06317 cell","definition":"[' NIGMS MAPPING PANEL #2, VERSION 3, HUMAN/RODENT SOMATIC CELL HYBRIDS']","term_type":"cell line"},{"accession":"CLO:0023132","name":"GM06318 cell","definition":"[' NIGMS MAPPING PANEL #2, VERSION 3, HUMAN/RODENT SOMATIC CELL HYBRIDS']","term_type":"cell line"},{"accession":"CLO:0023129","name":"GM06321 cell","definition":"[' TRANSLOCATED CHROMOSOME']","term_type":"cell line"},{"accession":"CLO:0023130","name":"GM06324 cell","definition":"[' NEUROAXONAL DYSTROPHY, INFANTILE']","term_type":"cell line"}]}