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{
"accession": "CLO:0023728",
"name": "GM10711 cell",
"definition": "[' ENDOGLIN; ENG TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER; HHT']",
"term_type": "cell line"
},
{
"accession": "CLO:0023732",
"name": "GM10712 cell",
"definition": "[' TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER; HHT']",
"term_type": "cell line"
},
{
"accession": "CLO:0023730",
"name": "GM10714 cell",
"definition": "[' TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER; HHT']",
"term_type": "cell line"
},
{
"accession": "CLO:0023718",
"name": "GM10715 cell",
"definition": "[' ENDOGLIN; ENG TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER; HHT']",
"term_type": "cell line"
},
{
"accession": "CLO:0023719",
"name": "GM10716 cell",
"definition": "[' TRANSLOCATED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0023716",
"name": "GM10717 cell",
"definition": "[' TRANSLOCATED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0023711",
"name": "GM10718 cell",
"definition": "[' SANDHOFF DISEASE']",
"term_type": "cell line"
},
{
"accession": "CLO:0023708",
"name": "GM10719 cell",
"definition": "[' SANDHOFF DISEASE']",
"term_type": "cell line"
},
{
"accession": "CLO:0023706",
"name": "GM10720 cell",
"definition": "[' SANDHOFF DISEASE']",
"term_type": "cell line"
},
{
"accession": "CLO:0023704",
"name": "GM10722 cell",
"definition": "[' CHROMOSOME DELETION']",
"term_type": "cell line"
},
{
"accession": "CLO:0023703",
"name": "GM10723 cell",
"definition": "[' MATURITY-ONSET DIABETES OF THE YOUNG, TYPE I; MODY1']",
"term_type": "cell line"
},
{
"accession": "CLO:0023702",
"name": "GM10724 cell",
"definition": "[' HEPATOCYTE NUCLEAR FACTOR 4-ALPHA; HNF4A MATURITY-ONSET DIABETES OF THE YOUNG, TYPE I; MODY1']",
"term_type": "cell line"
},
{
"accession": "CLO:0023701",
"name": "GM10725 cell",
"definition": "[' MATURITY-ONSET DIABETES OF THE YOUNG, TYPE I; MODY1']",
"term_type": "cell line"
},
{
"accession": "CLO:0023700",
"name": "GM10729 cell",
"definition": "[' MARFAN SYNDROME; MFS APPARENTLY HEALTHY NON-FETAL TISSUE']",
"term_type": "cell line"
},
{
"accession": "CLO:0023695",
"name": "GM10732 cell",
"definition": "[' ENDOGLIN; ENG TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER; HHT']",
"term_type": "cell line"
},
{
"accession": "CLO:0023698",
"name": "GM10742 cell",
"definition": "[' LEBER OPTIC ATROPHY COMPLEX I, SUBUNIT ND4; MTND4']",
"term_type": "cell line"
},
{
"accession": "CLO:0023683",
"name": "GM10744 cell",
"definition": "[' LEBER OPTIC ATROPHY COMPLEX I, SUBUNIT ND4; MTND4']",
"term_type": "cell line"
},
{
"accession": "CLO:0023675",
"name": "GM10748 cell",
"definition": "[' MARFAN SYNDROME; MFS']",
"term_type": "cell line"
},
{
"accession": "CLO:0023674",
"name": "GM10749 cell",
"definition": "[' THANATOPHORIC DYSPLASIA; TD FIBROBLAST GROWTH FACTOR RECEPTOR 3; FGFR3']",
"term_type": "cell line"
},
{
"accession": "CLO:0023679",
"name": "GM10763 cell",
"definition": "[' RING CHROMOSOME']",
"term_type": "cell line"
}
]
}