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{
"count": 43797,
"next": "https://cinder.proteo.info/api/ms_vocab/?format=api&limit=20&offset=14160&ordering=name",
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"results": [
{
"accession": "CLO:0016026",
"name": "GM03869 cell",
"definition": "[' HUNTINGTON DISEASE; HD']",
"term_type": "cell line"
},
{
"accession": "CLO:0016028",
"name": "GM03870 cell",
"definition": "[' HUNTINGTON DISEASE; HD']",
"term_type": "cell line"
},
{
"accession": "CLO:0016030",
"name": "GM03871 cell",
"definition": "[' HUNTINGTON DISEASE; HD']",
"term_type": "cell line"
},
{
"accession": "CLO:0016031",
"name": "GM03872 cell",
"definition": "[' HUNTINGTON DISEASE; HD']",
"term_type": "cell line"
},
{
"accession": "CLO:0016033",
"name": "GM03873 cell",
"definition": "[' HUNTINGTON DISEASE; HD']",
"term_type": "cell line"
},
{
"accession": "CLO:0016034",
"name": "GM03876 cell",
"definition": "[' TRANSLOCATED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0016037",
"name": "GM03877 cell",
"definition": "[' PYROGLUTAMICACIDURIA']",
"term_type": "cell line"
},
{
"accession": "CLO:0016038",
"name": "GM03878 cell",
"definition": "[' PYROGLUTAMICACIDURIA']",
"term_type": "cell line"
},
{
"accession": "CLO:0016041",
"name": "GM03882 cell",
"definition": "[' TRANSLOCATED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0016013",
"name": "GM03883 cell",
"definition": "[' INVERTED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0016011",
"name": "GM03884 cell",
"definition": "[' TRANSLOCATED CHROMOSOME KLIPPEL-FEIL SYNDROME; KFS; KFM CERVICAL VERTEBRAL FUSION, TYPE II, INCLUDED']",
"term_type": "cell line"
},
{
"accession": "CLO:0016012",
"name": "GM03886 cell",
"definition": "[' TRANSLOCATED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0016009",
"name": "GM03887 cell",
"definition": "[' CHROMOSOME DELETION']",
"term_type": "cell line"
},
{
"accession": "CLO:0016010",
"name": "GM03889 cell",
"definition": "[' USHER SYNDROME, TYPE IA; USH1A']",
"term_type": "cell line"
},
{
"accession": "CLO:0016007",
"name": "GM03890 cell",
"definition": "[' USHER SYNDROME, TYPE IA; USH1A']",
"term_type": "cell line"
},
{
"accession": "CLO:0016008",
"name": "GM03891 cell",
"definition": "[' USHER SYNDROME, TYPE IA; USH1A']",
"term_type": "cell line"
},
{
"accession": "CLO:0016022",
"name": "GM03892 cell",
"definition": "[' USHER SYNDROME, TYPE IA; USH1A']",
"term_type": "cell line"
},
{
"accession": "CLO:0016023",
"name": "GM03893 cell",
"definition": "[' RETINITIS PIGMENTOSA - 180100, 268000, OR 312600']",
"term_type": "cell line"
},
{
"accession": "CLO:0016018",
"name": "GM03894 cell",
"definition": "[' RETINITIS PIGMENTOSA - 180100, 268000, OR 312600']",
"term_type": "cell line"
},
{
"accession": "CLO:0015985",
"name": "GM03896 cell",
"definition": "[' REFSUM DISEASE']",
"term_type": "cell line"
}
]
}