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{
"count": 43797,
"next": "https://cinder.proteo.info/api/ms_vocab/?format=api&limit=20&offset=15180&ordering=name",
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"results": [
{
"accession": "CLO:0023094",
"name": "GM06228 cell",
"definition": "[' TRANSLOCATED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0023093",
"name": "GM06229 cell",
"definition": "[' TRANSLOCATED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0023095",
"name": "GM06230 cell",
"definition": "[' ANEUPLOID CHROMOSOME NUMBER - TRISOMY']",
"term_type": "cell line"
},
{
"accession": "CLO:0023106",
"name": "GM06231 cell",
"definition": "[' ZELLWEGER SYNDROME; ZS']",
"term_type": "cell line"
},
{
"accession": "CLO:0023107",
"name": "GM06246 cell",
"definition": "[' DICENTRIC CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0023108",
"name": "GM06248 cell",
"definition": "[' ALBUMIN; ALB DYSALBUMINEMIC HYPERTHYROXINEMIA, INCLUDED INVERTED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0023109",
"name": "GM06256 cell",
"definition": "[' ZELLWEGER SYNDROME; ZS INVERTED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0023110",
"name": "GM06260 cell",
"definition": "[' OSTEOGENESIS IMPERFECTA: GENETICS UNCERTAIN; LETHAL']",
"term_type": "cell line"
},
{
"accession": "CLO:0023111",
"name": "GM06261 cell",
"definition": "[' EHLERS-DANLOS SYNDROME: TYPE IV; ARTERIAL, ECCHYMOTIC TYPE']",
"term_type": "cell line"
},
{
"accession": "CLO:0023115",
"name": "GM06273 cell",
"definition": "[' HUNTINGTON DISEASE; HD']",
"term_type": "cell line"
},
{
"accession": "CLO:0023114",
"name": "GM06274 cell",
"definition": "[' HUNTINGTON DISEASE; HD']",
"term_type": "cell line"
},
{
"accession": "CLO:0023113",
"name": "GM06275 cell",
"definition": "[' TRANSLOCATED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0023112",
"name": "GM06312 cell",
"definition": "[' CHROMOSOME DELETION']",
"term_type": "cell line"
},
{
"accession": "CLO:0023128",
"name": "GM06314 cell",
"definition": "[' GLYCOGEN STORAGE DISEASE II GLUCOSIDASE, ALPHA, ACID; GAA']",
"term_type": "cell line"
},
{
"accession": "CLO:0023126",
"name": "GM06315 cell",
"definition": "[' APPARENTLY HEALTHY NON-FETAL TISSUE']",
"term_type": "cell line"
},
{
"accession": "CLO:0023127",
"name": "GM06316 cell",
"definition": "[' TRANSLOCATED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0023131",
"name": "GM06317 cell",
"definition": "[' NIGMS MAPPING PANEL #2, VERSION 3, HUMAN/RODENT SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
},
{
"accession": "CLO:0023132",
"name": "GM06318 cell",
"definition": "[' NIGMS MAPPING PANEL #2, VERSION 3, HUMAN/RODENT SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
},
{
"accession": "CLO:0023129",
"name": "GM06321 cell",
"definition": "[' TRANSLOCATED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0023130",
"name": "GM06324 cell",
"definition": "[' NEUROAXONAL DYSTROPHY, INFANTILE']",
"term_type": "cell line"
}
]
}