{"count":43797,"next":"https://cinder.proteo.info/api/ms_vocab/?format=json&limit=20&offset=13800&ordering=-accession","previous":"https://cinder.proteo.info/api/ms_vocab/?format=json&limit=20&offset=13760&ordering=-accession","results":[{"accession":"CLO:0029228","name":"GM10239 cell","definition":"[' TRANSLOCATED CHROMOSOME']","term_type":"cell line"},{"accession":"CLO:0029227","name":"ID00014 cell","definition":"[' DIGEORGE SYNDROME; DGS']","term_type":"cell line"},{"accession":"CLO:0029226","name":"GM10245 cell","definition":"[' EPIDERMOLYSIS BULLOSA: DYSTROPHIC, JUNCTIONAL, OR SIMPLEX TYPES']","term_type":"cell line"},{"accession":"CLO:0029225","name":"GM10247 cell","definition":"[' EPIDERMOLYSIS BULLOSA: DYSTROPHIC, JUNCTIONAL, OR SIMPLEX TYPES']","term_type":"cell line"},{"accession":"CLO:0029224","name":"ID00013 cell","definition":"[' COMMON VARIABLE IMMUNODEFICIENCY']","term_type":"cell line"},{"accession":"CLO:0029223","name":"ID00011 cell","definition":"[' COMMON VARIABLE IMMUNODEFICIENCY']","term_type":"cell line"},{"accession":"CLO:0029222","name":"GM10248 cell","definition":"[' TRANSLOCATED CHROMOSOME CORNELIA DE LANGE SYNDROME 1; CDLS1']","term_type":"cell line"},{"accession":"CLO:0029221","name":"ID00006 cell","definition":"[' COMMON VARIABLE IMMUNODEFICIENCY']","term_type":"cell line"},{"accession":"CLO:0029220","name":"GM10249 cell","definition":"[' TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER; HHT ENDOGLIN; ENG']","term_type":"cell line"},{"accession":"CLO:0029219","name":"ID00004 cell","definition":"[' WISKOTT-ALDRICH SYNDROME; WAS WAS GENE; WAS']","term_type":"cell line"},{"accession":"CLO:0029218","name":"GM10250 cell","definition":"[' TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER; HHT ENDOGLIN; ENG']","term_type":"cell line"},{"accession":"CLO:0029217","name":"GM10251 cell","definition":"[' SPINOCEREBELLAR ATAXIA 1; SCA1']","term_type":"cell line"},{"accession":"CLO:0029216","name":"GM10253 cell","definition":"[' NIGMS MAPPING PANEL #2, VERSION 3, HUMAN/RODENT SOMATIC CELL HYBRIDS']","term_type":"cell line"},{"accession":"CLO:0029215","name":"GM10254 cell","definition":"[' CHROMOSOME DELETION']","term_type":"cell line"},{"accession":"CLO:0029214","name":"ND06382 cell","definition":"[' SPOUSAL CONTROL']","term_type":"cell line"},{"accession":"CLO:0029213","name":"ID00034 cell","definition":"[' COMMON VARIABLE IMMUNODEFICIENCY']","term_type":"cell line"},{"accession":"CLO:0029212","name":"ND06397 cell","definition":"[\" PARKINSON'S DISEASE\"]","term_type":"cell line"},{"accession":"CLO:0029211","name":"GM10258 cell","definition":"[' EPIDERMOLYSIS BULLOSA: DYSTROPHIC, JUNCTIONAL, OR SIMPLEX TYPES']","term_type":"cell line"},{"accession":"CLO:0029210","name":"ID00030 cell","definition":"[' SPECIFIC ANTIBODY DEFICIENCY WITH NORMAL IMMUNOGLOBULINS AND PEG-TEETH']","term_type":"cell line"},{"accession":"CLO:0029209","name":"GM10259 cell","definition":"[' ASPHYXIATING THORACIC DYSTROPHY; ATD']","term_type":"cell line"}]}