{"count":43797,"next":"https://cinder.proteo.info/api/ms_vocab/?format=json&limit=20&offset=22560&ordering=-name","previous":"https://cinder.proteo.info/api/ms_vocab/?format=json&limit=20&offset=22520&ordering=-name","results":[{"accession":"CLO:0016185","name":"GM17897 cell","definition":"[' CLEIDOCRANIAL DYSPLASIA; CCD']","term_type":"cell line"},{"accession":"CLO:0016195","name":"GM17896 cell","definition":"[' CLEIDOCRANIAL DYSPLASIA; CCD']","term_type":"cell line"},{"accession":"CLO:0016149","name":"GM17895 cell","definition":"[' FRONTONASAL DYSPLASIA']","term_type":"cell line"},{"accession":"CLO:0016147","name":"GM17894 cell","definition":"[' NORMAL CHROMOSOMAL POLYMORPHISM APPARENTLY HEALTHY NON-FETAL TISSUE']","term_type":"cell line"},{"accession":"CLO:0016151","name":"GM17890 cell","definition":"[' ADAPTOR-RELATED PROTEIN COMPLEX 3, BETA-1 SUBUNIT; AP3B1 HERMANSKY-PUDLAK SYNDROME 2; HPS2']","term_type":"cell line"},{"accession":"CLO:0016150","name":"GM17888 cell","definition":"[' CYSTINOSIS, ADULT NONNEPHROPATHIC CYSTINOSIN; CTNS']","term_type":"cell line"},{"accession":"CLO:0016142","name":"GM17886 cell","definition":"[' CYSTINOSIS, NEPHROPATHIC; CTNS CYSTINOSIN; CTNS']","term_type":"cell line"},{"accession":"CLO:0016139","name":"GM17885 cell","definition":"[' CYSTINOSIN; CTNS CYSTINOSIS, NEPHROPATHIC; CTNS']","term_type":"cell line"},{"accession":"CLO:0016145","name":"GM17883 cell","definition":"[' XXY SYNDROME; KLINEFELTER SYNDROME ANEUPLOID CHROMOSOME NUMBER - NON-TRISOMIC']","term_type":"cell line"},{"accession":"CLO:0016143","name":"GM17881 cell","definition":"[' HERMANSKY-PUDLAK SYNDROME; HPS HERMANSKY-PUDLAK SYNDROME GENE 6']","term_type":"cell line"},{"accession":"CLO:0016152","name":"GM17880 cell","definition":"[' METHYL-CPG-BINDING PROTEIN 2; MECP2 RETT SYNDROME; RTT']","term_type":"cell line"},{"accession":"CLO:0016459","name":"GM17879 cell","definition":"[' ANEUPLOID CHROMOSOME NUMBER - NON-TRISOMIC XXY SYNDROME; KLINEFELTER SYNDROME']","term_type":"cell line"},{"accession":"CLO:0016460","name":"GM17869 cell","definition":"[' FSHD GENE 1; FRG1 FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1A;  FSHMD1A (FSHD)']","term_type":"cell line"},{"accession":"CLO:0016461","name":"GM17868 cell","definition":"[' FSHD GENE 1; FRG1 FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1A;  FSHMD1A (FSHD)']","term_type":"cell line"},{"accession":"CLO:0016462","name":"GM17867 cell","definition":"[' ANEUPLOID CHROMOSOME NUMBER - NON-TRISOMIC XXY SYNDROME; KLINEFELTER SYNDROME']","term_type":"cell line"},{"accession":"CLO:0016463","name":"GM17861 cell","definition":"[' XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC']","term_type":"cell line"},{"accession":"CLO:0016464","name":"GM17860 cell","definition":"[' XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC']","term_type":"cell line"},{"accession":"CLO:0016465","name":"GM17858 cell","definition":"[' XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC']","term_type":"cell line"},{"accession":"CLO:0016467","name":"GM17857 cell","definition":"[' ANEUPLOID CHROMOSOME NUMBER - NON-TRISOMIC XXY SYNDROME; KLINEFELTER SYNDROME']","term_type":"cell line"},{"accession":"CLO:0016466","name":"GM17856 cell","definition":"[' HUMAN VARIATION PANEL - HAN PEOPLE OF LOS ANGELES PANEL OF 100']","term_type":"cell line"}]}