HTTP 200 OK
Allow: GET, POST, HEAD, OPTIONS
Content-Type: application/json
Vary: Accept
{
"count": 43797,
"next": "https://cinder.proteo.info/api/ms_vocab/?format=api&limit=20&offset=13800&ordering=-accession",
"previous": "https://cinder.proteo.info/api/ms_vocab/?format=api&limit=20&offset=13760&ordering=-accession",
"results": [
{
"accession": "CLO:0029228",
"name": "GM10239 cell",
"definition": "[' TRANSLOCATED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0029227",
"name": "ID00014 cell",
"definition": "[' DIGEORGE SYNDROME; DGS']",
"term_type": "cell line"
},
{
"accession": "CLO:0029226",
"name": "GM10245 cell",
"definition": "[' EPIDERMOLYSIS BULLOSA: DYSTROPHIC, JUNCTIONAL, OR SIMPLEX TYPES']",
"term_type": "cell line"
},
{
"accession": "CLO:0029225",
"name": "GM10247 cell",
"definition": "[' EPIDERMOLYSIS BULLOSA: DYSTROPHIC, JUNCTIONAL, OR SIMPLEX TYPES']",
"term_type": "cell line"
},
{
"accession": "CLO:0029224",
"name": "ID00013 cell",
"definition": "[' COMMON VARIABLE IMMUNODEFICIENCY']",
"term_type": "cell line"
},
{
"accession": "CLO:0029223",
"name": "ID00011 cell",
"definition": "[' COMMON VARIABLE IMMUNODEFICIENCY']",
"term_type": "cell line"
},
{
"accession": "CLO:0029222",
"name": "GM10248 cell",
"definition": "[' TRANSLOCATED CHROMOSOME CORNELIA DE LANGE SYNDROME 1; CDLS1']",
"term_type": "cell line"
},
{
"accession": "CLO:0029221",
"name": "ID00006 cell",
"definition": "[' COMMON VARIABLE IMMUNODEFICIENCY']",
"term_type": "cell line"
},
{
"accession": "CLO:0029220",
"name": "GM10249 cell",
"definition": "[' TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER; HHT ENDOGLIN; ENG']",
"term_type": "cell line"
},
{
"accession": "CLO:0029219",
"name": "ID00004 cell",
"definition": "[' WISKOTT-ALDRICH SYNDROME; WAS WAS GENE; WAS']",
"term_type": "cell line"
},
{
"accession": "CLO:0029218",
"name": "GM10250 cell",
"definition": "[' TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER; HHT ENDOGLIN; ENG']",
"term_type": "cell line"
},
{
"accession": "CLO:0029217",
"name": "GM10251 cell",
"definition": "[' SPINOCEREBELLAR ATAXIA 1; SCA1']",
"term_type": "cell line"
},
{
"accession": "CLO:0029216",
"name": "GM10253 cell",
"definition": "[' NIGMS MAPPING PANEL #2, VERSION 3, HUMAN/RODENT SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
},
{
"accession": "CLO:0029215",
"name": "GM10254 cell",
"definition": "[' CHROMOSOME DELETION']",
"term_type": "cell line"
},
{
"accession": "CLO:0029214",
"name": "ND06382 cell",
"definition": "[' SPOUSAL CONTROL']",
"term_type": "cell line"
},
{
"accession": "CLO:0029213",
"name": "ID00034 cell",
"definition": "[' COMMON VARIABLE IMMUNODEFICIENCY']",
"term_type": "cell line"
},
{
"accession": "CLO:0029212",
"name": "ND06397 cell",
"definition": "[\" PARKINSON'S DISEASE\"]",
"term_type": "cell line"
},
{
"accession": "CLO:0029211",
"name": "GM10258 cell",
"definition": "[' EPIDERMOLYSIS BULLOSA: DYSTROPHIC, JUNCTIONAL, OR SIMPLEX TYPES']",
"term_type": "cell line"
},
{
"accession": "CLO:0029210",
"name": "ID00030 cell",
"definition": "[' SPECIFIC ANTIBODY DEFICIENCY WITH NORMAL IMMUNOGLOBULINS AND PEG-TEETH']",
"term_type": "cell line"
},
{
"accession": "CLO:0029209",
"name": "GM10259 cell",
"definition": "[' ASPHYXIATING THORACIC DYSTROPHY; ATD']",
"term_type": "cell line"
}
]
}