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{
"count": 43797,
"next": "https://cinder.proteo.info/api/ms_vocab/?format=api&limit=20&offset=18020&ordering=name",
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"results": [
{
"accession": "CLO:0019163",
"name": "GM12201 cell",
"definition": "[' PROTEUS SYNDROME']",
"term_type": "cell line"
},
{
"accession": "CLO:0019164",
"name": "GM12202 cell",
"definition": "[' PROTEUS SYNDROME']",
"term_type": "cell line"
},
{
"accession": "CLO:0019166",
"name": "GM12203 cell",
"definition": "[' PROTEUS SYNDROME']",
"term_type": "cell line"
},
{
"accession": "CLO:0019168",
"name": "GM12212 cell",
"definition": "[' PYRUVATE DECARBOXYLASE DEFICIENCY']",
"term_type": "cell line"
},
{
"accession": "CLO:0019169",
"name": "GM12214 cell",
"definition": "[' PERIPHERAL MYELIN PROTEIN 22; PMP22 CHARCOT-MARIE-TOOTH DISEASE, TYPE 1A; CMT1A']",
"term_type": "cell line"
},
{
"accession": "CLO:0019170",
"name": "GM12215 cell",
"definition": "[' ADDITIONAL DELETION/DERIVATIVE CHROMOSOME 17 SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
},
{
"accession": "CLO:0019181",
"name": "GM12217 cell",
"definition": "[' ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY']",
"term_type": "cell line"
},
{
"accession": "CLO:0019179",
"name": "GM12220 cell",
"definition": "[' SPONDYLOPERIPHERAL DYSPLASIA']",
"term_type": "cell line"
},
{
"accession": "CLO:0019180",
"name": "GM12221 cell",
"definition": "[' SPONDYLOPERIPHERAL DYSPLASIA']",
"term_type": "cell line"
},
{
"accession": "CLO:0019184",
"name": "GM12222 cell",
"definition": "[' HYPERAMMONEMIA DUE TO CARBAMOYLPHOSPHATE SYNTHETASE I DEFICIENCY']",
"term_type": "cell line"
},
{
"accession": "CLO:0019185",
"name": "GM12223 cell",
"definition": "[' HYPERAMMONEMIA DUE TO CARBAMOYLPHOSPHATE SYNTHETASE I DEFICIENCY']",
"term_type": "cell line"
},
{
"accession": "CLO:0019182",
"name": "GM12224 cell",
"definition": "[' HYPERAMMONEMIA DUE TO CARBAMOYLPHOSPHATE SYNTHETASE I DEFICIENCY']",
"term_type": "cell line"
},
{
"accession": "CLO:0019183",
"name": "GM12225 cell",
"definition": "[' INCONTINENTIA PIGMENTI; IP']",
"term_type": "cell line"
},
{
"accession": "CLO:0019187",
"name": "GM12226 cell",
"definition": "[' INCONTINENTIA PIGMENTI; IP']",
"term_type": "cell line"
},
{
"accession": "CLO:0019189",
"name": "GM12227 cell",
"definition": "[' ALAGILLE SYNDROME; AGS']",
"term_type": "cell line"
},
{
"accession": "CLO:0019186",
"name": "GM12228 cell",
"definition": "[' ALAGILLE SYNDROME; AGS']",
"term_type": "cell line"
},
{
"accession": "CLO:0019203",
"name": "GM12229 cell",
"definition": "[' CEPH/UTAH PEDIGREE 1375']",
"term_type": "cell line"
},
{
"accession": "CLO:0019204",
"name": "GM12230 cell",
"definition": "[' CEPH/UTAH PEDIGREE 1375']",
"term_type": "cell line"
},
{
"accession": "CLO:0019205",
"name": "GM12231 cell",
"definition": "[' CEPH/UTAH PEDIGREE 1375']",
"term_type": "cell line"
},
{
"accession": "CLO:0019206",
"name": "GM12232 cell",
"definition": "[' CEPH/UTAH PEDIGREE 1375']",
"term_type": "cell line"
}
]
}