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{
"count": 43797,
"next": "https://cinder.proteo.info/api/ms_vocab/?format=api&limit=20&offset=14900&ordering=name",
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"results": [
{
"accession": "CLO:0024648",
"name": "GM05700 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:0024647",
"name": "GM05726 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:0024640",
"name": "GM05740 cell",
"definition": "[' HUNTINGTON DISEASE; HD']",
"term_type": "cell line"
},
{
"accession": "CLO:0024637",
"name": "GM05747 cell",
"definition": "[' OSTEOGENESIS IMPERFECTA: GENETICS UNCERTAIN; LETHAL']",
"term_type": "cell line"
},
{
"accession": "CLO:0024638",
"name": "GM05748 cell",
"definition": "[' FARBER LIPOGRANULOMATOSIS']",
"term_type": "cell line"
},
{
"accession": "CLO:0024642",
"name": "GM05750 cell",
"definition": "[' CHROMOSOME INSERTION RETINOBLASTOMA, SPORADIC']",
"term_type": "cell line"
},
{
"accession": "CLO:0024644",
"name": "GM05751 cell",
"definition": "[' CHROMOSOME INSERTION RETINOBLASTOMA, SPORADIC']",
"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:0024665",
"name": "GM05754 cell",
"definition": "[' RING CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0024666",
"name": "GM05756 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:0024668",
"name": "GM05758 cell",
"definition": "[' APPARENTLY HEALTHY NON-FETAL TISSUE']",
"term_type": "cell line"
},
{
"accession": "CLO:0024658",
"name": "GM05759 cell",
"definition": "[' ALAGILLE SYNDROME; AGS']",
"term_type": "cell line"
},
{
"accession": "CLO:0024659",
"name": "GM05761 cell",
"definition": "[' WILSON DISEASE']",
"term_type": "cell line"
},
{
"accession": "CLO:0024660",
"name": "GM05762 cell",
"definition": "[' WILSON DISEASE']",
"term_type": "cell line"
},
{
"accession": "CLO:0024661",
"name": "GM05788 cell",
"definition": "[' SMITH-LEMLI-OPITZ SYNDROME, TYPE I']",
"term_type": "cell line"
},
{
"accession": "CLO:0024662",
"name": "GM05789 cell",
"definition": "[' SMITH-LEMLI-OPITZ SYNDROME, TYPE I']",
"term_type": "cell line"
}
]
}