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{
"count": 43797,
"next": "https://cinder.proteo.info/api/ms_vocab/?format=api&limit=20&offset=24320&ordering=-name",
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"results": [
{
"accession": "CLO:0031902",
"name": "GM14760 cell",
"definition": "[' POLYDACTYLY WITH NEONATAL CHONDRODYSTROPHY, TYPE II, MAJEWSKI TYPE']",
"term_type": "cell line"
},
{
"accession": "CLO:0031907",
"name": "GM14758 cell",
"definition": "[' POLYDACTYLY WITH NEONATAL CHONDRODYSTROPHY, TYPE II, MAJEWSKI TYPE']",
"term_type": "cell line"
},
{
"accession": "CLO:0031911",
"name": "GM14755 cell",
"definition": "[' APPARENTLY HEALTHY NON-FETAL TISSUE NON-OBESE CONTROLS']",
"term_type": "cell line"
},
{
"accession": "CLO:0031910",
"name": "GM14754 cell",
"definition": "[' APPARENTLY HEALTHY NON-FETAL TISSUE NON-OBESE CONTROLS']",
"term_type": "cell line"
},
{
"accession": "CLO:0031913",
"name": "GM14753 cell",
"definition": "[' APPARENTLY HEALTHY NON-FETAL TISSUE']",
"term_type": "cell line"
},
{
"accession": "CLO:0031912",
"name": "GM14746 cell",
"definition": "[' NON-OBESE CONTROLS APPARENTLY HEALTHY NON-FETAL TISSUE']",
"term_type": "cell line"
},
{
"accession": "CLO:0031915",
"name": "GM14734 cell",
"definition": "[' ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY']",
"term_type": "cell line"
},
{
"accession": "CLO:0031914",
"name": "GM14733 cell",
"definition": "[' ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY']",
"term_type": "cell line"
},
{
"accession": "CLO:0031917",
"name": "GM14732 cell",
"definition": "[' ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY']",
"term_type": "cell line"
},
{
"accession": "CLO:0031916",
"name": "GM14729 cell",
"definition": "[' LEOPARD SYNDROME']",
"term_type": "cell line"
},
{
"accession": "CLO:0031918",
"name": "GM14728 cell",
"definition": "[' LEOPARD SYNDROME']",
"term_type": "cell line"
},
{
"accession": "CLO:0031919",
"name": "GM14720 cell",
"definition": "[' APPARENTLY HEALTHY NON-FETAL TISSUE NON-OBESE CONTROLS']",
"term_type": "cell line"
},
{
"accession": "CLO:0031920",
"name": "GM14717 cell",
"definition": "[' NEURONAL INTRANUCLEAR INCLUSION DISEASE']",
"term_type": "cell line"
},
{
"accession": "CLO:0031994",
"name": "GM14715 cell",
"definition": "[' HEMOCHROMATOSIS; HFE']",
"term_type": "cell line"
},
{
"accession": "CLO:0031996",
"name": "GM14712 cell",
"definition": "[' HEMOCHROMATOSIS; HFE']",
"term_type": "cell line"
},
{
"accession": "CLO:0031991",
"name": "GM14707 cell",
"definition": "[' RHESUS BLOOD GROUP, D ANTIGEN; RHD']",
"term_type": "cell line"
},
{
"accession": "CLO:0031993",
"name": "GM14706 cell",
"definition": "[' RHESUS BLOOD GROUP, D ANTIGEN; RHD']",
"term_type": "cell line"
},
{
"accession": "CLO:0031989",
"name": "GM14704 cell",
"definition": "[' NON-OBESE CONTROLS APPARENTLY HEALTHY NON-FETAL TISSUE']",
"term_type": "cell line"
},
{
"accession": "CLO:0031990",
"name": "GM14703 cell",
"definition": "[' HEMOCHROMATOSIS; HFE']",
"term_type": "cell line"
},
{
"accession": "CLO:0031987",
"name": "GM14702 cell",
"definition": "[' PROTEASE INHIBITOR 1; PI HEMOCHROMATOSIS; HFE']",
"term_type": "cell line"
}
]
}