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{
"count": 43797,
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"results": [
{
"accession": "CLO:0024127",
"name": "GM10871 cell",
"definition": "[' GLUCOSIDASE, ACID BETA; GBA GAUCHER DISEASE, TYPE I']",
"term_type": "cell line"
},
{
"accession": "CLO:0024125",
"name": "GM10873 cell",
"definition": "[' GLUCOSIDASE, ACID BETA; GBA GAUCHER DISEASE, TYPE I']",
"term_type": "cell line"
},
{
"accession": "CLO:0024123",
"name": "GM10874 cell",
"definition": "[' GLUCOSIDASE, ACID BETA; GBA GAUCHER DISEASE, TYPE I']",
"term_type": "cell line"
},
{
"accession": "CLO:0024122",
"name": "GM10876 cell",
"definition": "[' WOLMAN DISEASE']",
"term_type": "cell line"
},
{
"accession": "CLO:0024119",
"name": "GM10879 cell",
"definition": "[' FRYNS SYNDROME; FRNS']",
"term_type": "cell line"
},
{
"accession": "CLO:0024118",
"name": "GM10880 cell",
"definition": "[' ADDITIONAL HUMAN/MOUSE SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
},
{
"accession": "CLO:0023418",
"name": "GM10881 cell",
"definition": "[' XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC']",
"term_type": "cell line"
},
{
"accession": "CLO:0023414",
"name": "GM10888 cell",
"definition": "[' ADDITIONAL DELETION/DERIVATIVE CHROMOSOME 22 SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
},
{
"accession": "CLO:0023415",
"name": "GM10889 cell",
"definition": "[' CHROMOSOME 17 REGIONAL MAPPING PANEL SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
},
{
"accession": "CLO:0023416",
"name": "GM10890 cell",
"definition": "[' CHROMOSOME 17 REGIONAL MAPPING PANEL SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
},
{
"accession": "CLO:0023417",
"name": "GM10892 cell",
"definition": "[' FIBROBLAST GROWTH FACTOR RECEPTOR 3; FGFR3 THANATOPHORIC DYSPLASIA; TD']",
"term_type": "cell line"
},
{
"accession": "CLO:0023413",
"name": "GM10893 cell",
"definition": "[' APPARENTLY HEALTHY NON-FETAL TISSUE THANATOPHORIC DYSPLASIA; TD']",
"term_type": "cell line"
},
{
"accession": "CLO:0023412",
"name": "GM10894 cell",
"definition": "[' APPARENTLY HEALTHY NON-FETAL TISSUE THANATOPHORIC DYSPLASIA; TD']",
"term_type": "cell line"
},
{
"accession": "CLO:0023411",
"name": "GM10897 cell",
"definition": "[' ADDITIONAL HUMAN/CHINESE HAMSTER SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
},
{
"accession": "CLO:0023410",
"name": "GM10898 cell",
"definition": "[' NIGMS MAPPING PANEL #2, VERSION 3, HUMAN/RODENT SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
},
{
"accession": "CLO:0023409",
"name": "GM10900 cell",
"definition": "[' XERODERMIC IDIOCY OF DE SANCTIS AND CACCHIONE EXCISION-REPAIR CROSS-COMPLEMENTING RODENT REPAIR DEFICIENCY, COMPLEMENTATION GROUP 6; ERCC6 COCKAYNE SYNDROME, TYPE B, INCLUDED; CSB, INCLUDED']",
"term_type": "cell line"
},
{
"accession": "CLO:0023397",
"name": "GM10901 cell",
"definition": "[' XERODERMIC IDIOCY OF DE SANCTIS AND CACCHIONE EXCISION-REPAIR CROSS-COMPLEMENTING RODENT REPAIR DEFICIENCY, COMPLEMENTATION GROUP 6; ERCC6 COCKAYNE SYNDROME, TYPE B, INCLUDED; CSB, INCLUDED']",
"term_type": "cell line"
},
{
"accession": "CLO:0023398",
"name": "GM10902 cell",
"definition": "[' XERODERMIC IDIOCY OF DE SANCTIS AND CACCHIONE EXCISION-REPAIR CROSS-COMPLEMENTING RODENT REPAIR DEFICIENCY, COMPLEMENTATION GROUP 6; ERCC6 COCKAYNE SYNDROME, TYPE B, INCLUDED; CSB, INCLUDED']",
"term_type": "cell line"
},
{
"accession": "CLO:0023395",
"name": "GM10903 cell",
"definition": "[' EXCISION-REPAIR CROSS-COMPLEMENTING RODENT REPAIR DEFICIENCY, COMPLEMENTATION GROUP 6; ERCC6 COCKAYNE SYNDROME, TYPE B, INCLUDED; CSB, INCLUDED XERODERMIC IDIOCY OF DE SANCTIS AND CACCHIONE']",
"term_type": "cell line"
},
{
"accession": "CLO:0023396",
"name": "GM10904 cell",
"definition": "[' XERODERMIC IDIOCY OF DE SANCTIS AND CACCHIONE EXCISION-REPAIR CROSS-COMPLEMENTING RODENT REPAIR DEFICIENCY, COMPLEMENTATION GROUP 6; ERCC6 COCKAYNE SYNDROME, TYPE B, INCLUDED; CSB, INCLUDED']",
"term_type": "cell line"
}
]
}