GET /api/ms_vocab/?format=api&offset=25040&ordering=-name
HTTP 200 OK
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{
    "count": 43797,
    "next": "https://cinder.proteo.info/api/ms_vocab/?format=api&limit=20&offset=25060&ordering=-name",
    "previous": "https://cinder.proteo.info/api/ms_vocab/?format=api&limit=20&offset=25020&ordering=-name",
    "results": [
        {
            "accession": "CLO:0012672",
            "name": "GM13428 cell",
            "definition": "[' MASA SYNDROME']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0012651",
            "name": "GM13427 cell",
            "definition": "[' PROCOLLAGEN-LYSINE, 2-OXOGLUTARATE 5-DIOXYGENASE; PLOD1 EHLERS-DANLOS SYNDROME, TYPE VI']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0012650",
            "name": "GM13426 cell",
            "definition": "[' PROCOLLAGEN-LYSINE, 2-OXOGLUTARATE 5-DIOXYGENASE; PLOD1 EHLERS-DANLOS SYNDROME, TYPE VI']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0012644",
            "name": "GM13425 cell",
            "definition": "[' PROCOLLAGEN-LYSINE, 2-OXOGLUTARATE 5-DIOXYGENASE; PLOD1 EHLERS-DANLOS SYNDROME, TYPE VI']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0012643",
            "name": "GM13423 cell",
            "definition": "[' CYSTIC FIBROSIS; CF CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; CFTR']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0012646",
            "name": "GM13419 cell",
            "definition": "[' BECKWITH-WIEDEMANN SYNDROME; BWS']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0012645",
            "name": "GM13418 cell",
            "definition": "[' BECKWITH-WIEDEMANN SYNDROME; BWS']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0012654",
            "name": "GM13416 cell",
            "definition": "[' BECKWITH-WIEDEMANN SYNDROME; BWS']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0012653",
            "name": "GM13415 cell",
            "definition": "[' BECKWITH-WIEDEMANN SYNDROME; BWS']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0012656",
            "name": "GM13413 cell",
            "definition": "[' CHROMOSOME 8 REGIONAL MAPPING PANEL SOMATIC CELL HYBRIDS']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0012655",
            "name": "GM13412 cell",
            "definition": "[' CHROMOSOME 8 REGIONAL MAPPING PANEL SOMATIC CELL HYBRIDS']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0012853",
            "name": "GM13411 cell",
            "definition": "[' ATP SYNTHASE 6; MTATP6 LEIGH SYNDROME']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0012856",
            "name": "GM13410 cell",
            "definition": "[' TRANSLOCATED CHROMOSOME']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0012849",
            "name": "GM13395 cell",
            "definition": "[' HOMOCYSTINURIA DUE TO DEFICIENCY OF N(5,10)-METHYLENETETRAHYDROFOLATE REDUCTASE ACTIVITY']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0012851",
            "name": "GM13371 cell",
            "definition": "[' XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP G; XPG']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0012846",
            "name": "GM13370 cell",
            "definition": "[' XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP G; XPG']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0012845",
            "name": "GM13365 cell",
            "definition": "[' ADRENAL HYPERPLASIA II']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0012844",
            "name": "GM13363 cell",
            "definition": "[' CHARCOT-MARIE-TOOTH DISEASE 1B; CMT1B MYELIN PROTEIN ZERO; MPZ']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0012843",
            "name": "GM13360 cell",
            "definition": "[' MYOTUBULAR MYOPATHY 1; MTM1']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0012842",
            "name": "GM13356 cell",
            "definition": "[' CEPH/VENEZUELAN PEDIGREE 104']",
            "term_type": "cell line"
        }
    ]
}