{"count":43797,"next":"https://cinder.proteo.info/api/ms_vocab/?format=json&limit=20&offset=13220&ordering=name","previous":"https://cinder.proteo.info/api/ms_vocab/?format=json&limit=20&offset=13180&ordering=name","results":[{"accession":"CLO:0032341","name":"GM01972 cell","definition":"[' HUTCHINSON-GILFORD PROGERIA SYNDROME; HGPS']","term_type":"cell line"},{"accession":"CLO:0032339","name":"GM01981 cell","definition":"[' MENKES SYNDROME ATPASE, CU(2+)-TRANSPORTING, ALPHA POLYPEPTIDE; ATP7A']","term_type":"cell line"},{"accession":"CLO:0032357","name":"GM01982 cell","definition":"[' MENKES SYNDROME ATPASE, CU(2+)-TRANSPORTING, ALPHA POLYPEPTIDE; ATP7A']","term_type":"cell line"},{"accession":"CLO:0032358","name":"GM01983 cell","definition":"[' MENKES SYNDROME']","term_type":"cell line"},{"accession":"CLO:0032355","name":"GM01984 cell","definition":"[' MENKES SYNDROME']","term_type":"cell line"},{"accession":"CLO:0032356","name":"GM01989 cell","definition":"[' APPARENTLY HEALTHY NON-FETAL TISSUE']","term_type":"cell line"},{"accession":"CLO:0032353","name":"GM01990 cell","definition":"[' APPARENTLY HEALTHY NON-FETAL TISSUE']","term_type":"cell line"},{"accession":"CLO:0032354","name":"GM01993 cell","definition":"[' ANEUPLOID CHROMOSOME NUMBER - NON-TRISOMIC']","term_type":"cell line"},{"accession":"CLO:0032281","name":"GM01995 cell","definition":"[' SITOSTEROLEMIA']","term_type":"cell line"},{"accession":"CLO:0032286","name":"GM01996 cell","definition":"[' GALACTOSEMIA GALACTOSE-1-PHOSPHATE URIDYLYLTRANSFERASE; GALT']","term_type":"cell line"},{"accession":"CLO:0032285","name":"GM01997 cell","definition":"[' ADENOSINE DEAMINASE; ADA 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:0032291","name":"GM01998 cell","definition":"[' TRANSTHYRETIN; TTR']","term_type":"cell line"},{"accession":"CLO:0032288","name":"GM01999 cell","definition":"[' TRANSTHYRETIN; TTR']","term_type":"cell line"},{"accession":"CLO:0032294","name":"GM02000 cell","definition":"[' HYPERCHOLESTEROLEMIA, FAMILIAL; FHC']","term_type":"cell line"},{"accession":"CLO:0032295","name":"GM02003 cell","definition":"[' CHROMOSOME DELETION']","term_type":"cell line"},{"accession":"CLO:0032296","name":"GM02004 cell","definition":"[' XERODERMA PIGMENTOSUM WITH NORMAL DNA REPAIR RATES']","term_type":"cell line"},{"accession":"CLO:0032297","name":"GM02007 cell","definition":"[' EHLERS-DANLOS SYNDROME, TYPE I; EDS1']","term_type":"cell line"},{"accession":"CLO:0032298","name":"GM02008 cell","definition":"[' CHROMOSOME DELETION']","term_type":"cell line"},{"accession":"CLO:0032301","name":"GM02009 cell","definition":"[' XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP A; XPA']","term_type":"cell line"},{"accession":"CLO:0032300","name":"GM02010 cell","definition":"[' XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP A; XPA']","term_type":"cell line"}]}