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{
"count": 43797,
"next": "https://cinder.proteo.info/api/ms_vocab/?format=api&limit=20&offset=6200&ordering=-accession",
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"results": [
{
"accession": "CLO:0036828",
"name": "GM07094 cell",
"definition": "[' LESCH-NYHAN SYNDROME; LNS']",
"term_type": "cell line"
},
{
"accession": "CLO:0036827",
"name": "GM07097 cell",
"definition": "[' MAJOR AFFECTIVE DISORDER - 125480 OR 309200']",
"term_type": "cell line"
},
{
"accession": "CLO:0036826",
"name": "GM07103 cell",
"definition": "[' SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE, B CELL-NEGATIVE, NK CELL-NEGATIVE, DUE TO ADENOSINE DEAMINASE DEFICIENCY ADENOSINE DEAMINASE; ADA']",
"term_type": "cell line"
},
{
"accession": "CLO:0036825",
"name": "GM07082 cell",
"definition": "[' TRANSLOCATED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0036824",
"name": "GM07087 cell",
"definition": "[' ACHROMATOPSIA 2; ACHM2']",
"term_type": "cell line"
},
{
"accession": "CLO:0036823",
"name": "GM07089 cell",
"definition": "[' EHLERS-DANLOS SYNDROME, TYPE II; EDS2']",
"term_type": "cell line"
},
{
"accession": "CLO:0036822",
"name": "GM07092 cell",
"definition": "[' LESCH-NYHAN SYNDROME; LNS HYPOXANTHINE GUANINE PHOSPHORIBOSYLTRANSFERASE 1; HPRT1; HPRT']",
"term_type": "cell line"
},
{
"accession": "CLO:0036821",
"name": "GM07078 cell",
"definition": "[' NIJMEGEN BREAKAGE SYNDROME GENE; NBS1 MARKER CHROMOSOME NIJMEGEN BREAKAGE SYNDROME']",
"term_type": "cell line"
},
{
"accession": "CLO:0036820",
"name": "GM07081 cell",
"definition": "[' TRANSLOCATED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0036819",
"name": "GM07149 cell",
"definition": "[' DICENTRIC CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0036818",
"name": "GM07147 cell",
"definition": "[' TRANSLOCATED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0036817",
"name": "GM07148 cell",
"definition": "[' CHROMOSOME DELETION']",
"term_type": "cell line"
},
{
"accession": "CLO:0036816",
"name": "GM07132 cell",
"definition": "[' FRAGILE SITE MENTAL RETARDATION 1; FMR1']",
"term_type": "cell line"
},
{
"accession": "CLO:0036815",
"name": "GM07146 cell",
"definition": "[' TRANSLOCATED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0036814",
"name": "GM07125 cell",
"definition": "[' RETICULOSIS, FAMILIAL HISTIOCYTIC']",
"term_type": "cell line"
},
{
"accession": "CLO:0036813",
"name": "GM07131 cell",
"definition": "[' FRAGILE SITE MENTAL RETARDATION 1; FMR1']",
"term_type": "cell line"
},
{
"accession": "CLO:0036812",
"name": "GM07106 cell",
"definition": "[' ANEUPLOID CHROMOSOME NUMBER - TRISOMY']",
"term_type": "cell line"
},
{
"accession": "CLO:0036811",
"name": "GM07114 cell",
"definition": "[' TRANSLOCATED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0036810",
"name": "GM07104 cell",
"definition": "[' SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE, B CELL-NEGATIVE, NK CELL-NEGATIVE, DUE TO ADENOSINE DEAMINASE DEFICIENCY']",
"term_type": "cell line"
},
{
"accession": "CLO:0036809",
"name": "GM07049 cell",
"definition": "[' CEPH/UTAH PEDIGREE 1333']",
"term_type": "cell line"
}
]
}