{"count":43797,"next":"https://cinder.proteo.info/api/ms_vocab/?format=json&limit=20&offset=6200&ordering=-accession","previous":"https://cinder.proteo.info/api/ms_vocab/?format=json&limit=20&offset=6160&ordering=-accession","results":[{"accession":"CLO:0036828","name":"GM07094 cell","definition":"[' LESCH-NYHAN SYNDROME; LNS']","term_type":"cell line"},{"accession":"CLO:0036827","name":"GM07097 cell","definition":"[' MAJOR AFFECTIVE DISORDER - 125480 OR 309200']","term_type":"cell line"},{"accession":"CLO:0036826","name":"GM07103 cell","definition":"[' SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE, B CELL-NEGATIVE, NK CELL-NEGATIVE, DUE TO ADENOSINE DEAMINASE DEFICIENCY ADENOSINE DEAMINASE; ADA']","term_type":"cell line"},{"accession":"CLO:0036825","name":"GM07082 cell","definition":"[' TRANSLOCATED CHROMOSOME']","term_type":"cell line"},{"accession":"CLO:0036824","name":"GM07087 cell","definition":"[' ACHROMATOPSIA 2; ACHM2']","term_type":"cell line"},{"accession":"CLO:0036823","name":"GM07089 cell","definition":"[' EHLERS-DANLOS SYNDROME, TYPE II; EDS2']","term_type":"cell line"},{"accession":"CLO:0036822","name":"GM07092 cell","definition":"[' LESCH-NYHAN SYNDROME; LNS HYPOXANTHINE GUANINE PHOSPHORIBOSYLTRANSFERASE 1; HPRT1; HPRT']","term_type":"cell line"},{"accession":"CLO:0036821","name":"GM07078 cell","definition":"[' NIJMEGEN BREAKAGE SYNDROME GENE; NBS1 MARKER CHROMOSOME NIJMEGEN BREAKAGE SYNDROME']","term_type":"cell line"},{"accession":"CLO:0036820","name":"GM07081 cell","definition":"[' TRANSLOCATED CHROMOSOME']","term_type":"cell line"},{"accession":"CLO:0036819","name":"GM07149 cell","definition":"[' DICENTRIC CHROMOSOME']","term_type":"cell line"},{"accession":"CLO:0036818","name":"GM07147 cell","definition":"[' TRANSLOCATED CHROMOSOME']","term_type":"cell line"},{"accession":"CLO:0036817","name":"GM07148 cell","definition":"[' CHROMOSOME DELETION']","term_type":"cell line"},{"accession":"CLO:0036816","name":"GM07132 cell","definition":"[' FRAGILE SITE MENTAL RETARDATION 1; FMR1']","term_type":"cell line"},{"accession":"CLO:0036815","name":"GM07146 cell","definition":"[' TRANSLOCATED CHROMOSOME']","term_type":"cell line"},{"accession":"CLO:0036814","name":"GM07125 cell","definition":"[' RETICULOSIS, FAMILIAL HISTIOCYTIC']","term_type":"cell line"},{"accession":"CLO:0036813","name":"GM07131 cell","definition":"[' FRAGILE SITE MENTAL RETARDATION 1; FMR1']","term_type":"cell line"},{"accession":"CLO:0036812","name":"GM07106 cell","definition":"[' ANEUPLOID CHROMOSOME NUMBER - TRISOMY']","term_type":"cell line"},{"accession":"CLO:0036811","name":"GM07114 cell","definition":"[' TRANSLOCATED CHROMOSOME']","term_type":"cell line"},{"accession":"CLO:0036810","name":"GM07104 cell","definition":"[' SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE, B CELL-NEGATIVE, NK CELL-NEGATIVE, DUE TO ADENOSINE DEAMINASE DEFICIENCY']","term_type":"cell line"},{"accession":"CLO:0036809","name":"GM07049 cell","definition":"[' CEPH/UTAH PEDIGREE 1333']","term_type":"cell line"}]}