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{
"count": 43797,
"next": "https://cinder.proteo.info/api/ms_vocab/?format=api&limit=20&offset=26700&ordering=-name",
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"results": [
{
"accession": "CLO:0024563",
"name": "GM10635 cell",
"definition": "[' TRANSLOCATED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0024564",
"name": "GM10634 cell",
"definition": "[' D-GLYCERICACIDEMIA']",
"term_type": "cell line"
},
{
"accession": "CLO:0024546",
"name": "GM10629 cell",
"definition": "[' ADDITIONAL HUMAN/CHINESE HAMSTER SOMATIC CELL HYBRIDS CHROMOSOME 12 REGIONAL MAPPING PANEL SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
},
{
"accession": "CLO:0024552",
"name": "GM10628 cell",
"definition": "[' THANATOPHORIC DYSPLASIA WITH KLEEBLATTSCHAEDEL']",
"term_type": "cell line"
},
{
"accession": "CLO:0024555",
"name": "GM10627 cell",
"definition": "[' THANATOPHORIC DYSPLASIA WITH KLEEBLATTSCHAEDEL']",
"term_type": "cell line"
},
{
"accession": "CLO:0024548",
"name": "GM10625 cell",
"definition": "[' LEBER OPTIC ATROPHY']",
"term_type": "cell line"
},
{
"accession": "CLO:0024550",
"name": "GM10624 cell",
"definition": "[' LEBER OPTIC ATROPHY']",
"term_type": "cell line"
},
{
"accession": "CLO:0024541",
"name": "GM10618 cell",
"definition": "[' USHER SYNDROME, TYPE IA; USH1A']",
"term_type": "cell line"
},
{
"accession": "CLO:0024542",
"name": "GM10614 cell",
"definition": "[' MARFAN SYNDROME; MFS']",
"term_type": "cell line"
},
{
"accession": "CLO:0024539",
"name": "GM10613 cell",
"definition": "[' TRANSLOCATED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0024540",
"name": "GM10612 cell",
"definition": "[' ADDITIONAL HUMAN/CHINESE HAMSTER SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
},
{
"accession": "CLO:0024543",
"name": "GM10611 cell",
"definition": "[' NIGMS MAPPING PANEL #2, VERSION 3, HUMAN/RODENT SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
},
{
"accession": "CLO:0024280",
"name": "GM10610 cell",
"definition": "[' HEMOGLOBIN--BETA LOCUS; HBB']",
"term_type": "cell line"
},
{
"accession": "CLO:0024279",
"name": "GM10609 cell",
"definition": "[' GREIG CEPHALOPOLYSYNDACTYLY SYNDROME; GCPS CHROMOSOME DELETION']",
"term_type": "cell line"
},
{
"accession": "CLO:0024284",
"name": "GM10608 cell",
"definition": "[' CHROMOSOME DELETION']",
"term_type": "cell line"
},
{
"accession": "CLO:0024283",
"name": "GM10607 cell",
"definition": "[' CHROMOSOME DELETION TRANSLOCATED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0024282",
"name": "GM10606 cell",
"definition": "[' TRIPLOID CHROMOSOME NUMBER']",
"term_type": "cell line"
},
{
"accession": "CLO:0024281",
"name": "GM10603 cell",
"definition": "[' TRANSLOCATED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0024288",
"name": "GM10570 cell",
"definition": "[' CEROID LIPOFUSCINOSIS, NEURONAL 2, LATE INFANTILE TYPE; CLN2']",
"term_type": "cell line"
},
{
"accession": "CLO:0024287",
"name": "GM10568 cell",
"definition": "[' DYGGVE-MELCHIOR-CLAUSEN DISEASE']",
"term_type": "cell line"
}
]
}