{"count":43797,"next":"https://cinder.proteo.info/api/ms_vocab/?format=json&limit=20&offset=15160&ordering=name","previous":"https://cinder.proteo.info/api/ms_vocab/?format=json&limit=20&offset=15120&ordering=name","results":[{"accession":"CLO:0023568","name":"GM06171 cell","definition":"[' APPARENTLY HEALTHY FETAL TISSUE']","term_type":"cell line"},{"accession":"CLO:0023569","name":"GM06172 cell","definition":"[' SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME']","term_type":"cell line"},{"accession":"CLO:0023570","name":"GM06174 cell","definition":"[' MAJOR AFFECTIVE DISORDER - 125480 OR 309200']","term_type":"cell line"},{"accession":"CLO:0023134","name":"GM06188 cell","definition":"[' TUBEROUS SCLEROSIS; TS TSC2 GENE; TSC2']","term_type":"cell line"},{"accession":"CLO:0023133","name":"GM06194 cell","definition":"[' TUBEROUS SCLEROSIS; TS']","term_type":"cell line"},{"accession":"CLO:0023136","name":"GM06195 cell","definition":"[' BARDET-BIEDL SYNDROME, BBS']","term_type":"cell line"},{"accession":"CLO:0023135","name":"GM06196 cell","definition":"[' BARDET-BIEDL SYNDROME, BBS']","term_type":"cell line"},{"accession":"CLO:0023141","name":"GM06197 cell","definition":"[' BARDET-BIEDL SYNDROME, BBS']","term_type":"cell line"},{"accession":"CLO:0023142","name":"GM06199 cell","definition":"[' RING CHROMOSOME']","term_type":"cell line"},{"accession":"CLO:0023139","name":"GM06200 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:0023140","name":"GM06201 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:0023137","name":"GM06206 cell","definition":"[' FELINE EHLERS-DANLOS SYNDROME: TYPE UNCLASSIFIED FELIS']","term_type":"cell line"},{"accession":"CLO:0023138","name":"GM06207 cell","definition":"[' FELIS']","term_type":"cell line"},{"accession":"CLO:0023147","name":"GM06214 cell","definition":"[' HURLER SYNDROME ALPHA-L-IDURONIDASE; IDUA']","term_type":"cell line"},{"accession":"CLO:0023146","name":"GM06221 cell","definition":"[' PROTOPORPHYRIA, ERYTHROPOIETIC']","term_type":"cell line"},{"accession":"CLO:0023145","name":"GM06222 cell","definition":"[' CHROMOSOME DELETION']","term_type":"cell line"},{"accession":"CLO:0023144","name":"GM06224 cell","definition":"[' KEARNS-SAYRE SYNDROME; KSS']","term_type":"cell line"},{"accession":"CLO:0023143","name":"GM06225 cell","definition":"[' KEARNS-SAYRE SYNDROME; KSS']","term_type":"cell line"},{"accession":"CLO:0023092","name":"GM06226 cell","definition":"[' TRANSLOCATED CHROMOSOME']","term_type":"cell line"},{"accession":"CLO:0023091","name":"GM06227 cell","definition":"[' TRANSLOCATED CHROMOSOME']","term_type":"cell line"}]}