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{
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"results": [
{
"accession": "CLO:0017455",
"name": "GM16659 cell",
"definition": "[' MULTIPLE ENDOCRINE NEOPLASIA, TYPE II; MEN2 RET PROTOONCOGENE; RET']",
"term_type": "cell line"
},
{
"accession": "CLO:0017359",
"name": "GM16658 cell",
"definition": "[' MULTIPLE ENDOCRINE NEOPLASIA, TYPE II; MEN2 RET PROTOONCOGENE; RET']",
"term_type": "cell line"
},
{
"accession": "CLO:0017363",
"name": "GM16654 cell",
"definition": "[' HUMAN VARIATION PANEL - CHINESE (VERSION 2) CHINESE POPULATION']",
"term_type": "cell line"
},
{
"accession": "CLO:0017362",
"name": "GM16643 cell",
"definition": "[' FACTOR V DEFICIENCY HEMOGLOBIN--BETA LOCUS; HBB']",
"term_type": "cell line"
},
{
"accession": "CLO:0017355",
"name": "GM16635 cell",
"definition": "[' FANCONI ANEMIA, COMPLEMENTATION GROUP G; FANCG X-RAY REPAIR, COMPLEMENTING DEFECTIVE, IN CHINESE HAMSTER, 9; XRCC9']",
"term_type": "cell line"
},
{
"accession": "CLO:0017354",
"name": "GM16634 cell",
"definition": "[' FANCONI ANEMIA, COMPLEMENTATION GROUP D2; FANCD2']",
"term_type": "cell line"
},
{
"accession": "CLO:0017357",
"name": "GM16633 cell",
"definition": "[' FANCONI ANEMIA, COMPLEMENTATION GROUP D2; FANCD2']",
"term_type": "cell line"
},
{
"accession": "CLO:0017356",
"name": "GM16632 cell",
"definition": "[' FANCONI ANEMIA, COMPLEMENTATION GROUP A; FANCA']",
"term_type": "cell line"
},
{
"accession": "CLO:0017351",
"name": "GM16631 cell",
"definition": "[' FANCONI ANEMIA, COMPLEMENTATION GROUP A; FANCA']",
"term_type": "cell line"
},
{
"accession": "CLO:0017349",
"name": "GM16627 cell",
"definition": "[' NEPHROSIS 1, CONGENITAL, FINNISH TYPE; NPHS1']",
"term_type": "cell line"
},
{
"accession": "CLO:0017352",
"name": "GM16599 cell",
"definition": "[' ADDITIONAL DELETION/DERIVATIVE CHROMOSOME 5 SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
},
{
"accession": "CLO:0017405",
"name": "GM16598 cell",
"definition": "[' CRI-DU-CHAT SYNDROME CHROMOSOME DELETION']",
"term_type": "cell line"
},
{
"accession": "CLO:0017403",
"name": "GM16595 cell",
"definition": "[' CRI-DU-CHAT SYNDROME CHROMOSOME DELETION']",
"term_type": "cell line"
},
{
"accession": "CLO:0017400",
"name": "GM16594 cell",
"definition": "[' ADDITIONAL DELETION/DERIVATIVE CHROMOSOME 5 SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
},
{
"accession": "CLO:0017398",
"name": "GM16593 cell",
"definition": "[' CHROMOSOME DELETION CRI-DU-CHAT SYNDROME']",
"term_type": "cell line"
},
{
"accession": "CLO:0017397",
"name": "GM16592 cell",
"definition": "[' ADDITIONAL DELETION/DERIVATIVE CHROMOSOME 5 SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
},
{
"accession": "CLO:0017396",
"name": "GM16590 cell",
"definition": "[' ADDITIONAL DELETION/DERIVATIVE CHROMOSOME 5 SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
},
{
"accession": "CLO:0017395",
"name": "GM16589 cell",
"definition": "[' ADDITIONAL DELETION/DERIVATIVE CHROMOSOME 5 SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
},
{
"accession": "CLO:0017394",
"name": "GM16588 cell",
"definition": "[' CRI-DU-CHAT SYNDROME']",
"term_type": "cell line"
},
{
"accession": "CLO:0017393",
"name": "GM16587 cell",
"definition": "[' ADDITIONAL DELETION/DERIVATIVE CHROMOSOME 18 SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
}
]
}