Ms Unique Vocabularies List

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{
    "count": 43797,
    "next": "https://cinder.proteo.info/api/ms_vocab/?format=api&limit=20&offset=26880&ordering=accession",
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    "results": [
        {
            "accession": "CLO:0026072",
            "name": "GM11349 cell",
            "definition": "[' RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 1; RCDP1']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0026073",
            "name": "GM11351 cell",
            "definition": "[' RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 1; RCDP1']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0026074",
            "name": "GM11370 cell",
            "definition": "[' CYSTIC FIBROSIS; CF CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; CFTR']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0026075",
            "name": "GM11373 cell",
            "definition": "[' CAMBODIAN POPULATION']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0026076",
            "name": "GM11376 cell",
            "definition": "[' CAMBODIAN POPULATION']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0026077",
            "name": "GM11377 cell",
            "definition": "[' CAMBODIAN POPULATION']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0026078",
            "name": "GM11338 cell",
            "definition": "[' RING CHROMOSOME']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0026079",
            "name": "GM11381 cell",
            "definition": "[' MAPLE SYRUP URINE DISEASE (MSUD), TYPE IA']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0026080",
            "name": "GM11382 cell",
            "definition": "[' PRADER-WILLI SYNDROME; PWS CHROMOSOME DELETION']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0026081",
            "name": "GM11380 cell",
            "definition": "[' INVERTED CHROMOSOME']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0026082",
            "name": "GM11390 cell",
            "definition": "[' PRADER-WILLI SYNDROME; PWS']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0026083",
            "name": "GM11388 cell",
            "definition": "[' PRADER-WILLI SYNDROME; PWS CHROMOSOME DELETION']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0026084",
            "name": "GM11389 cell",
            "definition": "[' PRADER-WILLI SYNDROME; PWS']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0026085",
            "name": "GM11386 cell",
            "definition": "[' PRADER-WILLI SYNDROME; PWS']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0026086",
            "name": "GM11387 cell",
            "definition": "[' PRADER-WILLI SYNDROME; PWS']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0026087",
            "name": "GM11383 cell",
            "definition": "[' PRADER-WILLI SYNDROME; PWS']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0026088",
            "name": "GM11385 cell",
            "definition": "[' CHROMOSOME DELETION PRADER-WILLI SYNDROME; PWS']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0026089",
            "name": "GM11391 cell",
            "definition": "[' PRADER-WILLI SYNDROME; PWS']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0026090",
            "name": "GM11392 cell",
            "definition": "[' PRADER-WILLI SYNDROME; PWS']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0026091",
            "name": "GM11393 cell",
            "definition": "[' PRADER-WILLI SYNDROME; PWS']",
            "term_type": "cell line"
        }
    ]
}