{"count":43797,"next":"https://cinder.proteo.info/api/ms_vocab/?format=json&limit=20&offset=13960&ordering=name","previous":"https://cinder.proteo.info/api/ms_vocab/?format=json&limit=20&offset=13920&ordering=name","results":[{"accession":"CLO:0017060","name":"GM03420 cell","definition":"[' NEUROFIBROMATOSIS, TYPE I; NF1']","term_type":"cell line"},{"accession":"CLO:0017059","name":"GM03421 cell","definition":"[' NEUROFIBROMATOSIS, TYPE I; NF1']","term_type":"cell line"},{"accession":"CLO:0017062","name":"GM03423 cell","definition":"[' TRANSLOCATED CHROMOSOME']","term_type":"cell line"},{"accession":"CLO:0017061","name":"GM03429 cell","definition":"[' MUSCULAR DYSTROPHY, PSEUDOHYPERTROPHIC PROGRESSIVE, DUCHENNE AND BECKER TYPES; DMD DYSTROPHIN; DMD']","term_type":"cell line"},{"accession":"CLO:0017065","name":"GM03432 cell","definition":"[' HYPERAMMONEMIA DUE TO CARBAMOYLPHOSPHATE SYNTHETASE I DEFICIENCY']","term_type":"cell line"},{"accession":"CLO:0017064","name":"GM03433 cell","definition":"[' HEMOGLOBIN--ALPHA LOCUS 2; HBA2']","term_type":"cell line"},{"accession":"CLO:0017049","name":"GM03435 cell","definition":"[' TRANSLOCATED CHROMOSOME']","term_type":"cell line"},{"accession":"CLO:0017047","name":"GM03440 cell","definition":"[' APPARENTLY HEALTHY NON-FETAL TISSUE']","term_type":"cell line"},{"accession":"CLO:0017035","name":"GM03441 cell","definition":"[' HEXOSAMINIDASE A; HEXA TAY-SACHS DISEASE; TSD']","term_type":"cell line"},{"accession":"CLO:0017034","name":"GM03459 cell","definition":"[' HYPOPHOSPHATASIA; PHOSPHOETHANOLAMINURIA - 241500 OR 241510']","term_type":"cell line"},{"accession":"CLO:0017033","name":"GM03461 cell","definition":"[' TAY-SACHS DISEASE; TSD HEXOSAMINIDASE A; HEXA']","term_type":"cell line"},{"accession":"CLO:0017032","name":"GM03462 cell","definition":"[' TRANSLOCATED CHROMOSOME']","term_type":"cell line"},{"accession":"CLO:0017031","name":"GM03463 cell","definition":"[' TRANSLOCATED CHROMOSOME']","term_type":"cell line"},{"accession":"CLO:0017030","name":"GM03465 cell","definition":"[' CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; CFTR CYSTIC FIBROSIS; CF']","term_type":"cell line"},{"accession":"CLO:0017029","name":"GM03466 cell","definition":"[' CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; CFTR CYSTIC FIBROSIS; CF']","term_type":"cell line"},{"accession":"CLO:0017028","name":"GM03467 cell","definition":"[' HYPOXANTHINE GUANINE PHOSPHORIBOSYLTRANSFERASE 1; HPRT1; HPRT LESCH-NYHAN SYNDROME; LNS']","term_type":"cell line"},{"accession":"CLO:0017027","name":"GM03468 cell","definition":"[' APPARENTLY HEALTHY NON-FETAL TISSUE']","term_type":"cell line"},{"accession":"CLO:0017026","name":"GM03469 cell","definition":"[' CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; CFTR APPARENTLY HEALTHY NON-FETAL TISSUE']","term_type":"cell line"},{"accession":"CLO:0017010","name":"GM03470 cell","definition":"[' CHROMOSOME DELETION']","term_type":"cell line"},{"accession":"CLO:0017012","name":"GM03478 cell","definition":"[' CORNELIA DE LANGE SYNDROME 1; CDLS1']","term_type":"cell line"}]}