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{
"count": 43797,
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"results": [
{
"accession": "CLO:0021452",
"name": "GM11754 cell",
"definition": "[' CHROMOSOME 3 REGIONAL MAPPING PANEL SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
},
{
"accession": "CLO:0021451",
"name": "GM11761 cell",
"definition": "[' CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; CFTR CYSTIC FIBROSIS; CF']",
"term_type": "cell line"
},
{
"accession": "CLO:0021450",
"name": "GM11762 cell",
"definition": "[' MUCOPOLYSACCHARIDOSIS TYPE IIIA']",
"term_type": "cell line"
},
{
"accession": "CLO:0021457",
"name": "GM11763 cell",
"definition": "[' GALACTOSE-1-PHOSPHATE URIDYLYLTRANSFERASE; GALT GALACTOSEMIA']",
"term_type": "cell line"
},
{
"accession": "CLO:0021456",
"name": "GM11764 cell",
"definition": "[' GALACTOSEMIA GALACTOSE-1-PHOSPHATE URIDYLYLTRANSFERASE; GALT']",
"term_type": "cell line"
},
{
"accession": "CLO:0021454",
"name": "GM11766 cell",
"definition": "[' CHROMOSOME 13 REGIONAL MAPPING PANEL SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
},
{
"accession": "CLO:0021400",
"name": "GM11767 cell",
"definition": "[' CHROMOSOME 13 REGIONAL MAPPING PANEL SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
},
{
"accession": "CLO:0021401",
"name": "GM11771 cell",
"definition": "[' TRANSLOCATED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0021402",
"name": "GM11776 cell",
"definition": "[' AMERINDIAN POPULATION']",
"term_type": "cell line"
},
{
"accession": "CLO:0021405",
"name": "GM11778 cell",
"definition": "[' WILSON DISEASE']",
"term_type": "cell line"
},
{
"accession": "CLO:0021421",
"name": "GM11779 cell",
"definition": "[' CHROMOSOME 8 REGIONAL MAPPING PANEL SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
},
{
"accession": "CLO:0021420",
"name": "GM11781 cell",
"definition": "[' ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY']",
"term_type": "cell line"
},
{
"accession": "CLO:0021423",
"name": "GM11811 cell",
"definition": "[' WILSON DISEASE']",
"term_type": "cell line"
},
{
"accession": "CLO:0021422",
"name": "GM11813 cell",
"definition": "[' SPONASTRIME DYSPLASIA']",
"term_type": "cell line"
},
{
"accession": "CLO:0021427",
"name": "GM11814 cell",
"definition": "[' SPONASTRIME DYSPLASIA']",
"term_type": "cell line"
},
{
"accession": "CLO:0021425",
"name": "GM11816 cell",
"definition": "[' OSTEOGENESIS IMPERFECTA: AUTOSOMAL DOMINANT- 166200,166210,166220, OR 166230']",
"term_type": "cell line"
},
{
"accession": "CLO:0021383",
"name": "GM11818 cell",
"definition": "[' CEPH/UTAH PEDIGREE 1331']",
"term_type": "cell line"
},
{
"accession": "CLO:0021381",
"name": "GM11819 cell",
"definition": "[' CEPH/UTAH PEDIGREE 1331']",
"term_type": "cell line"
},
{
"accession": "CLO:0021382",
"name": "GM11820 cell",
"definition": "[' CEPH/UTAH PEDIGREE 1333']",
"term_type": "cell line"
},
{
"accession": "CLO:0021379",
"name": "GM11821 cell",
"definition": "[' CEPH/UTAH PEDIGREE 1340']",
"term_type": "cell line"
}
]
}