Ms Unique Vocabularies List

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    "count": 43797,
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    "results": [
        {
            "accession": "CLO:0024659",
            "name": "GM05761 cell",
            "definition": "[' WILSON DISEASE']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0024658",
            "name": "GM05759 cell",
            "definition": "[' ALAGILLE SYNDROME; AGS']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0024668",
            "name": "GM05758 cell",
            "definition": "[' APPARENTLY HEALTHY NON-FETAL TISSUE']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0024667",
            "name": "GM05757 cell",
            "definition": "[' APPARENTLY HEALTHY NON-FETAL TISSUE']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0024666",
            "name": "GM05756 cell",
            "definition": "[' APPARENTLY HEALTHY NON-FETAL TISSUE']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0024665",
            "name": "GM05754 cell",
            "definition": "[' RING CHROMOSOME']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0024641",
            "name": "GM05752 cell",
            "definition": "[' FARBER LIPOGRANULOMATOSIS']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0003531",
            "name": "GM05752 cell",
            "definition": "[]",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0024644",
            "name": "GM05751 cell",
            "definition": "[' CHROMOSOME INSERTION RETINOBLASTOMA, SPORADIC']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0024642",
            "name": "GM05750 cell",
            "definition": "[' CHROMOSOME INSERTION RETINOBLASTOMA, SPORADIC']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0024638",
            "name": "GM05748 cell",
            "definition": "[' FARBER LIPOGRANULOMATOSIS']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0024637",
            "name": "GM05747 cell",
            "definition": "[' OSTEOGENESIS IMPERFECTA: GENETICS UNCERTAIN; LETHAL']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0024640",
            "name": "GM05740 cell",
            "definition": "[' HUNTINGTON DISEASE; HD']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0024639",
            "name": "GM05736 cell",
            "definition": "[' HUNTINGTON DISEASE; HD']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0024647",
            "name": "GM05726 cell",
            "definition": "[' HUNTINGTON DISEASE; HD']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0024646",
            "name": "GM05724 cell",
            "definition": "[' HUNTINGTON DISEASE; HD']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0024648",
            "name": "GM05700 cell",
            "definition": "[' HUNTINGTON DISEASE; HD']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0024621",
            "name": "GM05690 cell",
            "definition": "[' HUNTINGTON DISEASE; HD']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0024624",
            "name": "GM05688 cell",
            "definition": "[' HUNTINGTON DISEASE; HD']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0024619",
            "name": "GM05684 cell",
            "definition": "[' HUNTINGTON DISEASE; HD']",
            "term_type": "cell line"
        }
    ]
}