{"count":43797,"next":"https://cinder.proteo.info/api/ms_vocab/?format=json&limit=20&offset=26740&ordering=-accession","previous":"https://cinder.proteo.info/api/ms_vocab/?format=json&limit=20&offset=26700&ordering=-accession","results":[{"accession":"CLO:0016288","name":"GM17944 cell","definition":"[' COLLAGEN, TYPE I, ALPHA-2; COL1A2 OSTEOGENESIS IMPERFECTA, TYPE IV; OI4']","term_type":"cell line"},{"accession":"CLO:0016287","name":"GM17945 cell","definition":"[' OSTEOGENESIS IMPERFECTA, TYPE IV; OI4']","term_type":"cell line"},{"accession":"CLO:0016286","name":"GM17940 cell","definition":"[' FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1A;  FSHMD1A (FSHD) FSHD GENE 1; FRG1']","term_type":"cell line"},{"accession":"CLO:0016285","name":"GM17942 cell","definition":"[' DIGEORGE SYNDROME; DGS']","term_type":"cell line"},{"accession":"CLO:0016284","name":"GM17947 cell","definition":"[' COLLAGEN, TYPE I, ALPHA-2; COL1A2 OSTEOGENESIS IMPERFECTA, TYPE IV; OI4']","term_type":"cell line"},{"accession":"CLO:0016283","name":"GM17948 cell","definition":"[' OSTEOGENESIS IMPERFECTA, TYPE IV; OI4 COLLAGEN, TYPE I, ALPHA-2; COL1A2']","term_type":"cell line"},{"accession":"CLO:0016282","name":"GM17938 cell","definition":"[' VELOCARDIOFACIAL SYNDROME']","term_type":"cell line"},{"accession":"CLO:0016281","name":"GM17939 cell","definition":"[' FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1A;  FSHMD1A (FSHD) FSHD GENE 1; FRG1']","term_type":"cell line"},{"accession":"CLO:0016280","name":"GM17933 cell","definition":"[' CHROMOSOME DELETION']","term_type":"cell line"},{"accession":"CLO:0016279","name":"GM17934 cell","definition":"[' ANKYLOBLEPHARON-ECTODERMAL DEFECTS-CLEFT LIP/PALATE']","term_type":"cell line"},{"accession":"CLO:0016278","name":"GM17921 cell","definition":"[' NIEMANN-PICK DISEASE, TYPE C1; NPC1 NPC1 GENE; NPC1']","term_type":"cell line"},{"accession":"CLO:0016277","name":"GM17922 cell","definition":"[' NIEMANN-PICK DISEASE, TYPE C1; NPC1 NPC1 GENE; NPC1']","term_type":"cell line"},{"accession":"CLO:0016276","name":"GM17923 cell","definition":"[' NIEMANN-PICK DISEASE, TYPE C1; NPC1 NPC1 GENE; NPC1']","term_type":"cell line"},{"accession":"CLO:0016275","name":"GM17924 cell","definition":"[' NIEMANN-PICK DISEASE, TYPE C1; NPC1 NPC1 GENE; NPC1']","term_type":"cell line"},{"accession":"CLO:0016274","name":"GM17926 cell","definition":"[' NPC1 GENE; NPC1 NIEMANN-PICK DISEASE, TYPE C1; NPC1']","term_type":"cell line"},{"accession":"CLO:0016273","name":"GM17931 cell","definition":"[' XXY SYNDROME; KLINEFELTER SYNDROME ANEUPLOID CHROMOSOME NUMBER - NON-TRISOMIC']","term_type":"cell line"},{"accession":"CLO:0016272","name":"GM17932 cell","definition":"[' CEREBELLAR HYPOPLASIA']","term_type":"cell line"},{"accession":"CLO:0016271","name":"GM17918 cell","definition":"[' NPC1 GENE; NPC1 NIEMANN-PICK DISEASE, TYPE C1; NPC1']","term_type":"cell line"},{"accession":"CLO:0016270","name":"GM17919 cell","definition":"[' NPC1 GENE; NPC1 NIEMANN-PICK DISEASE, TYPE C1; NPC1']","term_type":"cell line"},{"accession":"CLO:0016269","name":"GM17920 cell","definition":"[' NPC1 GENE; NPC1 NIEMANN-PICK DISEASE, TYPE C1; NPC1']","term_type":"cell line"}]}