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{
"count": 43797,
"next": "https://cinder.proteo.info/api/ms_vocab/?format=api&limit=20&offset=12060&ordering=-accession",
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"results": [
{
"accession": "CLO:0030968",
"name": "GM01684 cell",
"definition": "[' CITRULLINEMIA']",
"term_type": "cell line"
},
{
"accession": "CLO:0030967",
"name": "GM01685 cell",
"definition": "[' CITRULLINEMIA']",
"term_type": "cell line"
},
{
"accession": "CLO:0030966",
"name": "GM01681 cell",
"definition": "[' APPARENTLY HEALTHY NON-FETAL TISSUE']",
"term_type": "cell line"
},
{
"accession": "CLO:0030965",
"name": "GM01683 cell",
"definition": "[' TRANSLOCATED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0030964",
"name": "GM01679 cell",
"definition": "[' CITRULLINEMIA']",
"term_type": "cell line"
},
{
"accession": "CLO:0030963",
"name": "GM01680 cell",
"definition": "[' APPARENTLY HEALTHY NON-FETAL TISSUE']",
"term_type": "cell line"
},
{
"accession": "CLO:0030962",
"name": "GM01676 cell",
"definition": "[' LOWE OCULOCEREBRORENAL SYNDROME; OCRL']",
"term_type": "cell line"
},
{
"accession": "CLO:0030961",
"name": "GM01678 cell",
"definition": "[' TRANSLOCATED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0030960",
"name": "GM01691 cell",
"definition": "[' EHLERS-DANLOS SYNDROME, TYPE II; EDS2']",
"term_type": "cell line"
},
{
"accession": "CLO:0030959",
"name": "GM01695 cell",
"definition": "[' MUSCULAR DYSTROPHY, PSEUDOHYPERTROPHIC PROGRESSIVE, DUCHENNE AND BECKER TYPES; DMD TRANSLOCATED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0030958",
"name": "GM01662 cell",
"definition": "[' HYPOXANTHINE GUANINE PHOSPHORIBOSYLTRANSFERASE 1; HPRT1; HPRT LESCH-NYHAN SYNDROME; LNS']",
"term_type": "cell line"
},
{
"accession": "CLO:0030957",
"name": "GM01663 cell",
"definition": "[' TRANSLOCATED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0030956",
"name": "GM01664 cell",
"definition": "[' TRANSLOCATED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0030955",
"name": "GM01665 cell",
"definition": "[' TRANSLOCATED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0030954",
"name": "GM01667 cell",
"definition": "[' CHROMOSOME DELETION']",
"term_type": "cell line"
},
{
"accession": "CLO:0030953",
"name": "GM01671 cell",
"definition": "[' CARTILAGE-HAIR HYPOPLASIA; CHH']",
"term_type": "cell line"
},
{
"accession": "CLO:0030952",
"name": "GM01672 cell",
"definition": "[' TRIPLOID CHROMOSOME NUMBER']",
"term_type": "cell line"
},
{
"accession": "CLO:0030951",
"name": "GM01673 cell",
"definition": "[' METHYLMALONICACIDURIA DUE TO METHYLMALONIC COA MUTASE DEFICIENCY']",
"term_type": "cell line"
},
{
"accession": "CLO:0030950",
"name": "GM01674 cell",
"definition": "[' METHYLMALONICACIDURIA, VITAMIN B12-RESPONSIVE, DUE TO DEFECT IN SYNTHESIS OF ADENOSYLCOBALAMIN--CBL A']",
"term_type": "cell line"
},
{
"accession": "CLO:0030949",
"name": "GM01675 cell",
"definition": "[' TAY-SACHS DISEASE, AB VARIANT']",
"term_type": "cell line"
}
]
}