{"count":43797,"next":"https://cinder.proteo.info/api/ms_vocab/?format=json&limit=20&offset=13420&ordering=name","previous":"https://cinder.proteo.info/api/ms_vocab/?format=json&limit=20&offset=13380&ordering=name","results":[{"accession":"CLO:0033122","name":"GM02337 cell","definition":"[' CHROMOSOME DELETION']","term_type":"cell line"},{"accession":"CLO:0033127","name":"GM02338 cell","definition":"[' LESCH-NYHAN SYNDROME; LNS']","term_type":"cell line"},{"accession":"CLO:0033118","name":"GM02339 cell","definition":"[' DYSTROPHIN; DMD MUSCULAR DYSTROPHY, PSEUDOHYPERTROPHIC PROGRESSIVE, DUCHENNE AND BECKER TYPES; DMD']","term_type":"cell line"},{"accession":"CLO:0033117","name":"GM02340 cell","definition":"[' HEMOGLOBIN--BETA LOCUS; HBB']","term_type":"cell line"},{"accession":"CLO:0033115","name":"GM02341 cell","definition":"[' NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE III; HSAN3']","term_type":"cell line"},{"accession":"CLO:0033116","name":"GM02342 cell","definition":"[' NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE III; HSAN3']","term_type":"cell line"},{"accession":"CLO:0033113","name":"GM02343 cell","definition":"[' ASPARTOACYLASE; ASPA INHIBITOR OF KAPPA LIGHT POLYPEPTIDE GENE ENHANCER IN B CELLS, KINASE-COMPLEX ASSOCIATED PROTEIN; IKBKAP NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE III; HSAN3']","term_type":"cell line"},{"accession":"CLO:0033114","name":"GM02344 cell","definition":"[' XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP A; XPA']","term_type":"cell line"},{"accession":"CLO:0033111","name":"GM02345 cell","definition":"[' XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP A; XPA']","term_type":"cell line"},{"accession":"CLO:0033112","name":"GM02346 cell","definition":"[' TRANSLOCATED CHROMOSOME']","term_type":"cell line"},{"accession":"CLO:0033109","name":"GM02347 cell","definition":"[' DYSTONIA 1, TORSION; DYT1']","term_type":"cell line"},{"accession":"CLO:0033110","name":"GM02355 cell","definition":"[' ADENOMATOUS POLYPOSIS OF THE COLON; APC (GARDNER SYNDROME INCLUDED)']","term_type":"cell line"},{"accession":"CLO:0033106","name":"GM02356 cell","definition":"[' CHROMOSOME DELETION']","term_type":"cell line"},{"accession":"CLO:0033108","name":"GM02359 cell","definition":"[' XERODERMA PIGMENTOSUM WITH NORMAL DNA REPAIR RATES']","term_type":"cell line"},{"accession":"CLO:0033107","name":"GM02361 cell","definition":"[' X-RAY REPAIR, COMPLEMENTING DEFECTIVE, IN CHINESE HAMSTER, 9; XRCC9 FANCONI ANEMIA, COMPLEMENTATION GROUP G; FANCG']","term_type":"cell line"},{"accession":"CLO:0033099","name":"GM02362 cell","definition":"[' FANCONI ANEMIA, COMPLEMENTATION GROUP A; FANCA']","term_type":"cell line"},{"accession":"CLO:0033100","name":"GM02363 cell","definition":"[' FANCONI ANEMIA, COMPLEMENTATION GROUP A; FANCA']","term_type":"cell line"},{"accession":"CLO:0033101","name":"GM02365 cell","definition":"[' COFFIN-LOWRY SYNDROME; CLS INVERTED CHROMOSOME']","term_type":"cell line"},{"accession":"CLO:0033102","name":"GM02366 cell","definition":"[' TAY-SACHS DISEASE; TSD HEXOSAMINIDASE A; HEXA ASPARTOACYLASE; ASPA']","term_type":"cell line"},{"accession":"CLO:0033103","name":"GM02373 cell","definition":"[' HYPERCHOLESTEROLEMIA, FAMILIAL; FHC']","term_type":"cell line"}]}