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{
"count": 43797,
"next": "https://cinder.proteo.info/api/ms_vocab/?format=api&limit=20&offset=25080&ordering=accession",
"previous": "https://cinder.proteo.info/api/ms_vocab/?format=api&limit=20&offset=25040&ordering=accession",
"results": [
{
"accession": "CLO:0024272",
"name": "GM10523 cell",
"definition": "[' RETINITIS PIGMENTOSA 1; RP1']",
"term_type": "cell line"
},
{
"accession": "CLO:0024273",
"name": "GM10524 cell",
"definition": "[' RETINITIS PIGMENTOSA 1; RP1']",
"term_type": "cell line"
},
{
"accession": "CLO:0024274",
"name": "GM10520 cell",
"definition": "[' RETINITIS PIGMENTOSA 1; RP1']",
"term_type": "cell line"
},
{
"accession": "CLO:0024275",
"name": "GM10521 cell",
"definition": "[' RETINITIS PIGMENTOSA 1; RP1']",
"term_type": "cell line"
},
{
"accession": "CLO:0024276",
"name": "GM10512 cell",
"definition": "[' MAJOR AFFECTIVE DISORDER; OLD ORDER AMISH - 125480 OR 309200']",
"term_type": "cell line"
},
{
"accession": "CLO:0024277",
"name": "GM10511 cell",
"definition": "[' MAJOR AFFECTIVE DISORDER; OLD ORDER AMISH - 125480 OR 309200']",
"term_type": "cell line"
},
{
"accession": "CLO:0024278",
"name": "GM10510 cell",
"definition": "[' MAJOR AFFECTIVE DISORDER; OLD ORDER AMISH - 125480 OR 309200']",
"term_type": "cell line"
},
{
"accession": "CLO:0024279",
"name": "GM10609 cell",
"definition": "[' GREIG CEPHALOPOLYSYNDACTYLY SYNDROME; GCPS CHROMOSOME DELETION']",
"term_type": "cell line"
},
{
"accession": "CLO:0024280",
"name": "GM10610 cell",
"definition": "[' HEMOGLOBIN--BETA LOCUS; HBB']",
"term_type": "cell line"
},
{
"accession": "CLO:0024281",
"name": "GM10603 cell",
"definition": "[' TRANSLOCATED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0024282",
"name": "GM10606 cell",
"definition": "[' TRIPLOID CHROMOSOME NUMBER']",
"term_type": "cell line"
},
{
"accession": "CLO:0024283",
"name": "GM10607 cell",
"definition": "[' CHROMOSOME DELETION TRANSLOCATED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0024284",
"name": "GM10608 cell",
"definition": "[' CHROMOSOME DELETION']",
"term_type": "cell line"
},
{
"accession": "CLO:0024285",
"name": "GM10566 cell",
"definition": "[' MARFAN SYNDROME; MFS']",
"term_type": "cell line"
},
{
"accession": "CLO:0024286",
"name": "GM10567 cell",
"definition": "[' NIGMS MAPPING PANEL #2, VERSION 3, HUMAN/RODENT SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
},
{
"accession": "CLO:0024287",
"name": "GM10568 cell",
"definition": "[' DYGGVE-MELCHIOR-CLAUSEN DISEASE']",
"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:0024289",
"name": "GM10565 cell",
"definition": "[' TRANSLOCATED CHROMOSOME KALLMANN SYN; HYPOGONADOTROPIC HYPOGONADISM, ANOSMIA- 147950, 244200, 308700']",
"term_type": "cell line"
},
{
"accession": "CLO:0024290",
"name": "GM10557 cell",
"definition": "[' ANEUPLOID CHROMOSOME NUMBER - TRISOMY']",
"term_type": "cell line"
},
{
"accession": "CLO:0024291",
"name": "GM10559 cell",
"definition": "[' MARFAN SYNDROME; MFS']",
"term_type": "cell line"
}
]
}