{"count":43797,"next":"https://cinder.proteo.info/api/ms_vocab/?format=json&limit=20&offset=11300&ordering=accession","previous":"https://cinder.proteo.info/api/ms_vocab/?format=json&limit=20&offset=11260&ordering=accession","results":[{"accession":"CLO:0010492","name":"GM08763 cell","definition":"[' CHROMOSOME DELETION']","term_type":"cell line"},{"accession":"CLO:0010493","name":"GM08761 cell","definition":"[' CYSTINOSIS, ADULT NONNEPHROPATHIC']","term_type":"cell line"},{"accession":"CLO:0010494","name":"GM08766 cell","definition":"[' MULTIPLE ENDOCRINE NEOPLASIA, TYPE II; MEN2']","term_type":"cell line"},{"accession":"CLO:0010495","name":"GM08764 cell","definition":"[' ZELLWEGER SYNDROME; ZS']","term_type":"cell line"},{"accession":"CLO:0010496","name":"GM08769 cell","definition":"[' REFSUM DISEASE, INFANTILE FORM']","term_type":"cell line"},{"accession":"CLO:0010497","name":"GM08768 cell","definition":"[' ACYL-COA DEHYDROGENASE, MEDIUM-CHAIN; ACADM ACYL-CoA DEHYDROGENASE, MEDIUM-CHAIN, DEFICIENCY OF']","term_type":"cell line"},{"accession":"CLO:0010498","name":"GM08771 cell","definition":"[' PEROXISOME BIOGENESIS FACTOR 26; PEX26 REFSUM DISEASE, INFANTILE FORM']","term_type":"cell line"},{"accession":"CLO:0010499","name":"GM08770 cell","definition":"[' REFSUM DISEASE, INFANTILE FORM']","term_type":"cell line"},{"accession":"CLO:0010500","name":"GM08739 cell","definition":"[' POLYCYSTIC KIDNEYS']","term_type":"cell line"},{"accession":"CLO:0010501","name":"GM08740 cell","definition":"[' POLYCYSTIC KIDNEYS']","term_type":"cell line"},{"accession":"CLO:0010502","name":"GM08728 cell","definition":"[' DNA METHYLTRANSFERASE 3B; DNMT3B APPARENTLY HEALTHY NON-FETAL TISSUE IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME']","term_type":"cell line"},{"accession":"CLO:0010503","name":"GM08729 cell","definition":"[' IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME APPARENTLY HEALTHY NON-FETAL TISSUE']","term_type":"cell line"},{"accession":"CLO:0010504","name":"GM08752 cell","definition":"[' GAUCHER DISEASE, TYPE II GLUCOSIDASE, ACID BETA; GBA']","term_type":"cell line"},{"accession":"CLO:0010505","name":"GM08747 cell","definition":"[' IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME DNA METHYLTRANSFERASE 3B; DNMT3B']","term_type":"cell line"},{"accession":"CLO:0010506","name":"GM08741 cell","definition":"[' POLYCYSTIC KIDNEYS']","term_type":"cell line"},{"accession":"CLO:0010507","name":"GM08757 cell","definition":"[' MATURITY-ONSET DIABETES OF THE YOUNG, TYPE I; MODY1']","term_type":"cell line"},{"accession":"CLO:0010508","name":"GM08756 cell","definition":"[' MATURITY-ONSET DIABETES OF THE YOUNG, TYPE I; MODY1']","term_type":"cell line"},{"accession":"CLO:0010509","name":"GM08755 cell","definition":"[' TRANSLOCATED CHROMOSOME']","term_type":"cell line"},{"accession":"CLO:0010510","name":"GM08753 cell","definition":"[' GLUCOSIDASE, ACID BETA; GBA GAUCHER DISEASE, TYPE II']","term_type":"cell line"},{"accession":"CLO:0010511","name":"GM08880 cell","definition":"[' MAJOR AFFECTIVE DISORDER; OLD ORDER AMISH - 125480 OR 309200']","term_type":"cell line"}]}