{"count":43797,"next":"https://cinder.proteo.info/api/ms_vocab/?format=json&limit=20&offset=28380&ordering=-name","previous":"https://cinder.proteo.info/api/ms_vocab/?format=json&limit=20&offset=28340&ordering=-name","results":[{"accession":"CLO:0036814","name":"GM07125 cell","definition":"[' RETICULOSIS, FAMILIAL HISTIOCYTIC']","term_type":"cell line"},{"accession":"CLO:0036811","name":"GM07114 cell","definition":"[' TRANSLOCATED CHROMOSOME']","term_type":"cell line"},{"accession":"CLO:0036812","name":"GM07106 cell","definition":"[' ANEUPLOID CHROMOSOME NUMBER - TRISOMY']","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: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:0036827","name":"GM07097 cell","definition":"[' MAJOR AFFECTIVE DISORDER - 125480 OR 309200']","term_type":"cell line"},{"accession":"CLO:0036828","name":"GM07094 cell","definition":"[' LESCH-NYHAN SYNDROME; LNS']","term_type":"cell line"},{"accession":"CLO:0036829","name":"GM07093 cell","definition":"[' LESCH-NYHAN SYNDROME; LNS']","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:0036823","name":"GM07089 cell","definition":"[' EHLERS-DANLOS SYNDROME, TYPE II; EDS2']","term_type":"cell line"},{"accession":"CLO:0036824","name":"GM07087 cell","definition":"[' ACHROMATOPSIA 2; ACHM2']","term_type":"cell line"},{"accession":"CLO:0036825","name":"GM07082 cell","definition":"[' TRANSLOCATED CHROMOSOME']","term_type":"cell line"},{"accession":"CLO:0036820","name":"GM07081 cell","definition":"[' TRANSLOCATED CHROMOSOME']","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:0036830","name":"GM07077 cell","definition":"[' PORPHYRIA, ACUTE INTERMITTENT']","term_type":"cell line"},{"accession":"CLO:0036791","name":"GM07072 cell","definition":"[' FRAGILE SITE MENTAL RETARDATION 1; FMR1 CHROMOSOME DELETION']","term_type":"cell line"},{"accession":"CLO:0036792","name":"GM07071 cell","definition":"[' FRAGILE SITE MENTAL RETARDATION 1; FMR1']","term_type":"cell line"},{"accession":"CLO:0036789","name":"GM07069 cell","definition":"[' TRANSLOCATED CHROMOSOME']","term_type":"cell line"},{"accession":"CLO:0036790","name":"GM07067 cell","definition":"[' LETTERER-SIWE DISEASE']","term_type":"cell line"},{"accession":"CLO:0036795","name":"GM07065 cell","definition":"[' ICHTHYOSIS CONGENITA, HARLEQUIN FETUS TYPE']","term_type":"cell line"}]}