HTTP 200 OK
Allow: GET, POST, HEAD, OPTIONS
Content-Type: application/json
Vary: Accept
{
"count": 43797,
"next": "https://cinder.proteo.info/api/ms_vocab/?format=api&limit=20&offset=17700&ordering=name",
"previous": "https://cinder.proteo.info/api/ms_vocab/?format=api&limit=20&offset=17660&ordering=name",
"results": [
{
"accession": "CLO:0021360",
"name": "GM11629 cell",
"definition": "[' NEUROMATA, MUCOSAL, WITH ENDOCRINE TUMORS']",
"term_type": "cell line"
},
{
"accession": "CLO:0021354",
"name": "GM11630 cell",
"definition": "[' MULTIPLE ENDOCRINE NEOPLASIA, TYPE I; MEN1']",
"term_type": "cell line"
},
{
"accession": "CLO:0021357",
"name": "GM11631 cell",
"definition": "[' MULTIPLE ENDOCRINE NEOPLASIA, TYPE I; MEN1']",
"term_type": "cell line"
},
{
"accession": "CLO:0021365",
"name": "GM11632 cell",
"definition": "[' ICHTHYOSIS CONGENITA, HARLEQUIN FETUS TYPE']",
"term_type": "cell line"
},
{
"accession": "CLO:0021368",
"name": "GM11633 cell",
"definition": "[' ICHTHYOSIS CONGENITA, HARLEQUIN FETUS TYPE']",
"term_type": "cell line"
},
{
"accession": "CLO:0021362",
"name": "GM11634 cell",
"definition": "[' ARGININEMIA']",
"term_type": "cell line"
},
{
"accession": "CLO:0021319",
"name": "GM11635 cell",
"definition": "[' XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC']",
"term_type": "cell line"
},
{
"accession": "CLO:0021321",
"name": "GM11636 cell",
"definition": "[' XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC']",
"term_type": "cell line"
},
{
"accession": "CLO:0021323",
"name": "GM11637 cell",
"definition": "[' XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC']",
"term_type": "cell line"
},
{
"accession": "CLO:0021324",
"name": "GM11638 cell",
"definition": "[' XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC']",
"term_type": "cell line"
},
{
"accession": "CLO:0021326",
"name": "GM11639 cell",
"definition": "[' XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC']",
"term_type": "cell line"
},
{
"accession": "CLO:0021329",
"name": "GM11654 cell",
"definition": "[' EWING SARCOMA BREAKPOINT REGION 1; EWSR1, INCLUDED; EWS, INCLUDED; ES, INCLUDED TRANSLOCATED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0021330",
"name": "GM11661 cell",
"definition": "[' GLYCOGEN STORAGE DISEASE II GLUCOSIDASE, ALPHA, ACID; GAA']",
"term_type": "cell line"
},
{
"accession": "CLO:0021332",
"name": "GM11672 cell",
"definition": "[' CHROMOSOME DELETION']",
"term_type": "cell line"
},
{
"accession": "CLO:0021335",
"name": "GM11675 cell",
"definition": "[' INVERTED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0021336",
"name": "GM11677 cell",
"definition": "[' OSTEOGENESIS IMPERFECTA: AUTOSOMAL DOMINANT- 166200,166210,166220, OR 166230']",
"term_type": "cell line"
},
{
"accession": "CLO:0021285",
"name": "GM11678 cell",
"definition": "[' TRANSLOCATED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0021302",
"name": "GM11679 cell",
"definition": "[' ADDITIONAL HUMAN/MOUSE SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
},
{
"accession": "CLO:0021304",
"name": "GM11685 cell",
"definition": "[' ADDITIONAL DELETION/DERIVATIVE CHROMOSOME 17 SOMATIC CELL HYBRIDS CHROMOSOME 22 REGIONAL MAPPING PANEL SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
},
{
"accession": "CLO:0021298",
"name": "GM11686 cell",
"definition": "[' ADDITIONAL HUMAN/MOUSE SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
}
]
}