{"count":43797,"next":"https://cinder.proteo.info/api/ms_vocab/?format=json&limit=20&offset=32620&ordering=accession","previous":"https://cinder.proteo.info/api/ms_vocab/?format=json&limit=20&offset=32580&ordering=accession","results":[{"accession":"CLO:0031812","name":"HQ00792 cell","definition":"[' HUNTINGTON DISEASE; HD']","term_type":"cell line"},{"accession":"CLO:0031813","name":"HQ00800 cell","definition":"[' HUNTINGTON DISEASE; HD']","term_type":"cell line"},{"accession":"CLO:0031814","name":"HQ00797 cell","definition":"[' HUNTINGTON DISEASE; HD']","term_type":"cell line"},{"accession":"CLO:0031815","name":"HQ00798 cell","definition":"[' HUNTINGTON DISEASE; HD']","term_type":"cell line"},{"accession":"CLO:0031816","name":"HQ00788 cell","definition":"[' HUNTINGTON DISEASE; HD']","term_type":"cell line"},{"accession":"CLO:0031817","name":"HQ00789 cell","definition":"[' HUNTINGTON DISEASE; HD']","term_type":"cell line"},{"accession":"CLO:0031818","name":"HQ00786 cell","definition":"[' HUNTINGTON DISEASE; HD']","term_type":"cell line"},{"accession":"CLO:0031819","name":"GM02109 cell","definition":"[' WOLMAN DISEASE']","term_type":"cell line"},{"accession":"CLO:0031820","name":"GM02103 cell","definition":"[' TRANSLOCATED CHROMOSOME']","term_type":"cell line"},{"accession":"CLO:0031821","name":"GM02096 cell","definition":"[' XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC']","term_type":"cell line"},{"accession":"CLO:0031822","name":"GM02095 cell","definition":"[' METACHROMATIC LEUKODYSTROPHY, LATE-INFANTILE']","term_type":"cell line"},{"accession":"CLO:0031823","name":"GM02099 cell","definition":"[' BASAL CELL NEVUS SYNDROME; BCNS']","term_type":"cell line"},{"accession":"CLO:0031824","name":"GM02098 cell","definition":"[' BASAL CELL NEVUS SYNDROME; BCNS']","term_type":"cell line"},{"accession":"CLO:0031825","name":"GM02091 cell","definition":"[' XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP A; XPA']","term_type":"cell line"},{"accession":"CLO:0031826","name":"GM02090 cell","definition":"[' XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP A; XPA']","term_type":"cell line"},{"accession":"CLO:0031827","name":"GM02094 cell","definition":"[' SANDHOFF DISEASE']","term_type":"cell line"},{"accession":"CLO:0031828","name":"GM02093 cell","definition":"[' METACHROMATIC LEUKODYSTROPHY, LATE-INFANTILE']","term_type":"cell line"},{"accession":"CLO:0031829","name":"HQ00778 cell","definition":"[' HUNTINGTON DISEASE; HD']","term_type":"cell line"},{"accession":"CLO:0031830","name":"GM02110 cell","definition":"[' HYPERCHOLESTEROLEMIA, FAMILIAL; FHC']","term_type":"cell line"},{"accession":"CLO:0031831","name":"HQ00779 cell","definition":"[' HUNTINGTON DISEASE; HD']","term_type":"cell line"}]}