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{
"accession": "CLO:0010691",
"name": "GM09212 cell",
"definition": "[' MAJOR AFFECTIVE DISORDER; OLD ORDER AMISH - 125480 OR 309200']",
"term_type": "cell line"
},
{
"accession": "CLO:0010692",
"name": "GM09211 cell",
"definition": "[' MAJOR AFFECTIVE DISORDER; OLD ORDER AMISH - 125480 OR 309200']",
"term_type": "cell line"
},
{
"accession": "CLO:0010688",
"name": "GM09210 cell",
"definition": "[' MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS CHROMOSOME DELETION']",
"term_type": "cell line"
},
{
"accession": "CLO:0010636",
"name": "GM09209 cell",
"definition": "[' MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS CHROMOSOME DELETION']",
"term_type": "cell line"
},
{
"accession": "CLO:0010635",
"name": "GM09208 cell",
"definition": "[' MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS CHROMOSOME DELETION']",
"term_type": "cell line"
},
{
"accession": "CLO:0010640",
"name": "GM09197 cell",
"definition": "[' HUNTINGTON DISEASE; HD']",
"term_type": "cell line"
},
{
"accession": "CLO:0010639",
"name": "GM09196 cell",
"definition": "[' MENKES SYNDROME']",
"term_type": "cell line"
},
{
"accession": "CLO:0010638",
"name": "GM09195 cell",
"definition": "[' MENKES SYNDROME']",
"term_type": "cell line"
},
{
"accession": "CLO:0010637",
"name": "GM09194 cell",
"definition": "[' MENKES SYNDROME']",
"term_type": "cell line"
},
{
"accession": "CLO:0010634",
"name": "GM09193 cell",
"definition": "[' MAJOR AFFECTIVE DISORDER; OLD ORDER AMISH - 125480 OR 309200']",
"term_type": "cell line"
},
{
"accession": "CLO:0010633",
"name": "GM09192 cell",
"definition": "[' TRANSLOCATED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0010632",
"name": "GM09191 cell",
"definition": "[' CHROMOSOME 6 REGIONAL MAPPING PANEL SOMATIC CELL HYBRIDS ADDITIONAL DELETION/DERIVATIVE X CHROMOSOME SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
},
{
"accession": "CLO:0010631",
"name": "GM09189 cell",
"definition": "[' PRADER-WILLI SYNDROME; PWS CHROMOSOME DELETION']",
"term_type": "cell line"
},
{
"accession": "CLO:0010624",
"name": "GM09154 cell",
"definition": "[' NEUROAXONAL DYSTROPHY, INFANTILE']",
"term_type": "cell line"
},
{
"accession": "CLO:0010626",
"name": "GM09153 cell",
"definition": "[' HEMOGLOBIN--BETA LOCUS; HBB']",
"term_type": "cell line"
},
{
"accession": "CLO:0010625",
"name": "GM09146 cell",
"definition": "[' FRAGILE SITE MENTAL RETARDATION 1; FMR1']",
"term_type": "cell line"
},
{
"accession": "CLO:0010628",
"name": "GM09145 cell",
"definition": "[' FRAGILE SITE MENTAL RETARDATION 1; FMR1']",
"term_type": "cell line"
},
{
"accession": "CLO:0010627",
"name": "GM09142 cell",
"definition": "[' CHROMOSOME 21 REGIONAL MAPPING PANEL SOMATIC CELL HYBRIDS CHROMOSOME X REGIONAL MAPPING PANEL SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
},
{
"accession": "CLO:0010630",
"name": "GM09138 cell",
"definition": "[' MAJOR AFFECTIVE DISORDER; OLD ORDER AMISH - 125480 OR 309200']",
"term_type": "cell line"
},
{
"accession": "CLO:0010629",
"name": "GM09133 cell",
"definition": "[' CHROMOSOME DELETION PRADER-WILLI SYNDROME; PWS']",
"term_type": "cell line"
}
]
}