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{
"count": 43797,
"next": "https://cinder.proteo.info/api/ms_vocab/?format=api&limit=20&offset=27460&ordering=-name",
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"results": [
{
"accession": "CLO:0012022",
"name": "GM09256 cell",
"definition": "[' VON HIPPEL-LINDAU SYNDROME; VHL']",
"term_type": "cell line"
},
{
"accession": "CLO:0012021",
"name": "GM09255 cell",
"definition": "[' APPARENTLY HEALTHY NON-FETAL TISSUE VON HIPPEL-LINDAU SYNDROME; VHL']",
"term_type": "cell line"
},
{
"accession": "CLO:0012020",
"name": "GM09254 cell",
"definition": "[' ATAXIA-TELANGIECTASIA; AT']",
"term_type": "cell line"
},
{
"accession": "CLO:0012036",
"name": "GM09252 cell",
"definition": "[' ATAXIA-TELANGIECTASIA; AT']",
"term_type": "cell line"
},
{
"accession": "CLO:0012031",
"name": "GM09247 cell",
"definition": "[' ATAXIA-TELANGIECTASIA; AT']",
"term_type": "cell line"
},
{
"accession": "CLO:0012033",
"name": "GM09246 cell",
"definition": "[' ATAXIA-TELANGIECTASIA; AT']",
"term_type": "cell line"
},
{
"accession": "CLO:0012039",
"name": "GM09239 cell",
"definition": "[' PORPHYRIA, ACUTE INTERMITTENT']",
"term_type": "cell line"
},
{
"accession": "CLO:0012040",
"name": "GM09238 cell",
"definition": "[' FRAGILE SITE MENTAL RETARDATION 1; FMR1']",
"term_type": "cell line"
},
{
"accession": "CLO:0012037",
"name": "GM09237 cell",
"definition": "[' FRAGILE SITE MENTAL RETARDATION 1; FMR1']",
"term_type": "cell line"
},
{
"accession": "CLO:0012038",
"name": "GM09236 cell",
"definition": "[' FRAGILE SITE MENTAL RETARDATION 1; FMR1']",
"term_type": "cell line"
},
{
"accession": "CLO:0012008",
"name": "GM09232 cell",
"definition": "[' APPARENTLY HEALTHY NON-FETAL TISSUE MENKES SYNDROME']",
"term_type": "cell line"
},
{
"accession": "CLO:0012007",
"name": "GM09231 cell",
"definition": "[' MENKES SYNDROME']",
"term_type": "cell line"
},
{
"accession": "CLO:0012009",
"name": "GM09230 cell",
"definition": "[' MENKES SYNDROME']",
"term_type": "cell line"
},
{
"accession": "CLO:0010687",
"name": "GM09229 cell",
"definition": "[' RING CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0010683",
"name": "GM09218 cell",
"definition": "[' CRIGLER-NAJJAR SYNDROME UDP-GLYCOSYLTRANSFERASE 1 FAMILY, POLYPEPTIDE A1; UGT1A1']",
"term_type": "cell line"
},
{
"accession": "CLO:0010684",
"name": "GM09217 cell",
"definition": "[' CRIGLER-NAJJAR SYNDROME UDP-GLYCOSYLTRANSFERASE 1 FAMILY, POLYPEPTIDE A1; UGT1A1']",
"term_type": "cell line"
},
{
"accession": "CLO:0010685",
"name": "GM09216 cell",
"definition": "[' CHROMOSOME DELETION']",
"term_type": "cell line"
},
{
"accession": "CLO:0010686",
"name": "GM09215 cell",
"definition": "[' MAJOR AFFECTIVE DISORDER; OLD ORDER AMISH - 125480 OR 309200']",
"term_type": "cell line"
},
{
"accession": "CLO:0010689",
"name": "GM09214 cell",
"definition": "[' MAJOR AFFECTIVE DISORDER; OLD ORDER AMISH - 125480 OR 309200']",
"term_type": "cell line"
},
{
"accession": "CLO:0010690",
"name": "GM09213 cell",
"definition": "[' MAJOR AFFECTIVE DISORDER; OLD ORDER AMISH - 125480 OR 309200']",
"term_type": "cell line"
}
]
}