GET /api/ms_vocab/?format=api&offset=17120&ordering=name
HTTP 200 OK
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Vary: Accept

{
    "count": 43797,
    "next": "https://cinder.proteo.info/api/ms_vocab/?format=api&limit=20&offset=17140&ordering=name",
    "previous": "https://cinder.proteo.info/api/ms_vocab/?format=api&limit=20&offset=17100&ordering=name",
    "results": [
        {
            "accession": "CLO:0024559",
            "name": "GM10642 cell",
            "definition": "[' SJOGREN-LARSSON SYNDROME']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0024575",
            "name": "GM10647 cell",
            "definition": "[' OSTEOCHONDRODYSPLASIA WITH RHIZOMELIA & OTHER FEATURES - UNKNOWN INHERITANCE']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0024574",
            "name": "GM10648 cell",
            "definition": "[' OSTEOCHONDRODYSPLASIA WITH RHIZOMELIA & OTHER FEATURES - UNKNOWN INHERITANCE']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0024572",
            "name": "GM10650 cell",
            "definition": "[' GLUTARICACIDEMIA I']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0024570",
            "name": "GM10652 cell",
            "definition": "[' GLUTARICACIDEMIA I']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0024579",
            "name": "GM10653 cell",
            "definition": "[' GLUTARICACIDEMIA I']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0024582",
            "name": "GM10657 cell",
            "definition": "[' CHROMOSOME 17 REGIONAL MAPPING PANEL SOMATIC CELL HYBRIDS']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0024581",
            "name": "GM10658 cell",
            "definition": "[' CRICETULUS']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0024584",
            "name": "GM10659 cell",
            "definition": "[' CHROMOSOME 17 REGIONAL MAPPING PANEL SOMATIC CELL HYBRIDS CHROMOSOME 15 REGIONAL MAPPING PANEL SOMATIC CELL HYBRIDS']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0024583",
            "name": "GM10660 cell",
            "definition": "[' CHROMOSOME 17 REGIONAL MAPPING PANEL SOMATIC CELL HYBRIDS CHROMOSOME 1 REGIONAL MAPPING PANEL SOMATIC CELL HYBRIDS']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0024586",
            "name": "GM10662 cell",
            "definition": "[' CHROMOSOME X REGIONAL MAPPING PANEL SOMATIC CELL HYBRIDS']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0024585",
            "name": "GM10663 cell",
            "definition": "[' CHROMOSOME X REGIONAL MAPPING PANEL SOMATIC CELL HYBRIDS']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0024589",
            "name": "GM10664 cell",
            "definition": "[' CHROMOSOME 10 REGIONAL MAPPING PANEL SOMATIC CELL HYBRIDS CHROMOSOME 15 REGIONAL MAPPING PANEL SOMATIC CELL HYBRIDS']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0024588",
            "name": "GM10665 cell",
            "definition": "[' CARNITINE DEFICIENCY, SYSTEMIC PRIMARY; CDSP']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0024592",
            "name": "GM10666 cell",
            "definition": "[' CARNITINE DEFICIENCY, SYSTEMIC PRIMARY; CDSP']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0024610",
            "name": "GM10667 cell",
            "definition": "[' CARNITINE DEFICIENCY, SYSTEMIC PRIMARY; CDSP']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0024606",
            "name": "GM10668 cell",
            "definition": "[' MATURITY-ONSET DIABETES OF THE YOUNG, TYPE I; MODY1 HEPATOCYTE NUCLEAR FACTOR 4-ALPHA; HNF4A']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0024605",
            "name": "GM10669 cell",
            "definition": "[' COWDEN DISEASE; CD']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0024603",
            "name": "GM10672 cell",
            "definition": "[' CEROID LIPOFUSCINOSIS, NEURONAL 2, LATE INFANTILE TYPE; CLN2']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0024618",
            "name": "GM10679 cell",
            "definition": "[' ANEUPLOID CHROMOSOME NUMBER - NON-TRISOMIC']",
            "term_type": "cell line"
        }
    ]
}