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{
"count": 43797,
"next": "https://cinder.proteo.info/api/ms_vocab/?format=api&limit=20&offset=25120&ordering=-name",
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"results": [
{
"accession": "CLO:0013352",
"name": "GM13287 cell",
"definition": "[' TRICHOTHIODYSTROPHY; TTD ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH RETARDATION, INCLUDED']",
"term_type": "cell line"
},
{
"accession": "CLO:0013300",
"name": "GM13286 cell",
"definition": "[' TRICHOTHIODYSTROPHY; TTD ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH RETARDATION, INCLUDED']",
"term_type": "cell line"
},
{
"accession": "CLO:0013286",
"name": "GM13284 cell",
"definition": "[' TRANSLOCATED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0013283",
"name": "GM13281 cell",
"definition": "[' 5Q- MYELODYSPLASIA']",
"term_type": "cell line"
},
{
"accession": "CLO:0013282",
"name": "GM13280 cell",
"definition": "[' TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER; HHT']",
"term_type": "cell line"
},
{
"accession": "CLO:0013279",
"name": "GM13278 cell",
"definition": "[' LIPASE, CONGENITAL ABSENCE OF PANCREATIC']",
"term_type": "cell line"
},
{
"accession": "CLO:0013290",
"name": "GM13277 cell",
"definition": "[' CHROMOSOME DELETION']",
"term_type": "cell line"
},
{
"accession": "CLO:0013289",
"name": "GM13276 cell",
"definition": "[' VAS DEFERENS, CONGENITAL BILATERAL APLASIA OF; CBAVD']",
"term_type": "cell line"
},
{
"accession": "CLO:0013288",
"name": "GM13275 cell",
"definition": "[' ACYL-CoA DEHYDROGENASE, MEDIUM-CHAIN, DEFICIENCY OF ACYL-COA DEHYDROGENASE, MEDIUM-CHAIN; ACADM']",
"term_type": "cell line"
},
{
"accession": "CLO:0013287",
"name": "GM13273 cell",
"definition": "[' ZELLWEGER SYNDROME; ZS']",
"term_type": "cell line"
},
{
"accession": "CLO:0013313",
"name": "GM13272 cell",
"definition": "[' ZELLWEGER SYNDROME; ZS']",
"term_type": "cell line"
},
{
"accession": "CLO:0013105",
"name": "GM13269 cell",
"definition": "[' ZELLWEGER SYNDROME; ZS']",
"term_type": "cell line"
},
{
"accession": "CLO:0013108",
"name": "GM13268 cell",
"definition": "[' ADRENOLEUKODYSTROPHY, AUTOSOMAL NEONATAL FORM']",
"term_type": "cell line"
},
{
"accession": "CLO:0013123",
"name": "GM13267 cell",
"definition": "[' ZELLWEGER SYNDROME; ZS']",
"term_type": "cell line"
},
{
"accession": "CLO:0013126",
"name": "GM13266 cell",
"definition": "[' ZELLWEGER SYNDROME; ZS']",
"term_type": "cell line"
},
{
"accession": "CLO:0013129",
"name": "GM13265 cell",
"definition": "[' PEROXISOMAL BIFUNCTIONAL ENZYME DEFICIENCY']",
"term_type": "cell line"
},
{
"accession": "CLO:0013134",
"name": "GM13264 cell",
"definition": "[' PEROXISOMAL BIFUNCTIONAL ENZYME DEFICIENCY 17-@BETA-HYDROXYSTEROID DEHYDROGENASE IV; HSD17B4']",
"term_type": "cell line"
},
{
"accession": "CLO:0013114",
"name": "GM13263 cell",
"definition": "[' 17-@BETA-HYDROXYSTEROID DEHYDROGENASE IV; HSD17B4 PEROXISOMAL BIFUNCTIONAL ENZYME DEFICIENCY']",
"term_type": "cell line"
},
{
"accession": "CLO:0013116",
"name": "GM13262 cell",
"definition": "[' PEROXISOMAL BIFUNCTIONAL ENZYME DEFICIENCY']",
"term_type": "cell line"
},
{
"accession": "CLO:0013119",
"name": "GM13260 cell",
"definition": "[' ADDITIONAL HUMAN/MOUSE SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
}
]
}