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=25040&ordering=accession",
"previous": "https://cinder.proteo.info/api/ms_vocab/?format=api&limit=20&offset=25000&ordering=accession",
"results": [
{
"accession": "CLO:0024232",
"name": "GM05870 cell",
"definition": "[' ACYL-COA DEHYDROGENASE, MEDIUM-CHAIN; ACADM ACYL-CoA DEHYDROGENASE, MEDIUM-CHAIN, DEFICIENCY OF']",
"term_type": "cell line"
},
{
"accession": "CLO:0024233",
"name": "GM05864 cell",
"definition": "[' BOVINE PROTOPORPHYRIA BOS']",
"term_type": "cell line"
},
{
"accession": "CLO:0024234",
"name": "GM05866 cell",
"definition": "[' BOVINE PORPHYRIA, CONGENITAL ERYTHROPOIETIC BOS']",
"term_type": "cell line"
},
{
"accession": "CLO:0024235",
"name": "GM05865 cell",
"definition": "[' BOVINE PROTOPORPHYRIA BOS']",
"term_type": "cell line"
},
{
"accession": "CLO:0024236",
"name": "GM05876 cell",
"definition": "[' DIGEORGE SYNDROME; DGS']",
"term_type": "cell line"
},
{
"accession": "CLO:0024237",
"name": "GM05875 cell",
"definition": "[' CHROMOSOME DELETION']",
"term_type": "cell line"
},
{
"accession": "CLO:0024238",
"name": "GM05877 cell",
"definition": "[' CHROMOSOME DELETION RETINOBLASTOMA, SPORADIC']",
"term_type": "cell line"
},
{
"accession": "CLO:0024239",
"name": "GM10506 cell",
"definition": "[' USHER SYNDROME, TYPE IA; USH1A']",
"term_type": "cell line"
},
{
"accession": "CLO:0024240",
"name": "GM10505 cell",
"definition": "[' USHER SYNDROME, TYPE IA; USH1A']",
"term_type": "cell line"
},
{
"accession": "CLO:0024241",
"name": "GM10509 cell",
"definition": "[' MAJOR AFFECTIVE DISORDER; OLD ORDER AMISH - 125480 OR 309200']",
"term_type": "cell line"
},
{
"accession": "CLO:0024242",
"name": "GM10507 cell",
"definition": "[' HYPOPHOSPHATASIA; PHOSPHOETHANOLAMINURIA - 241500 OR 241510']",
"term_type": "cell line"
},
{
"accession": "CLO:0024243",
"name": "GM10501 cell",
"definition": "[' CHROMOSOME 17 REGIONAL MAPPING PANEL SOMATIC CELL HYBRIDS CHROMOSOME X REGIONAL MAPPING PANEL SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
},
{
"accession": "CLO:0024244",
"name": "GM10500 cell",
"definition": "[' CHROMOSOME 17 REGIONAL MAPPING PANEL SOMATIC CELL HYBRIDS CHROMOSOME 15 REGIONAL MAPPING PANEL SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
},
{
"accession": "CLO:0024245",
"name": "GM10503 cell",
"definition": "[' COLLAGEN, TYPE I, ALPHA-2; COL1A2 OSTEOGENESIS IMPERFECTA: GENETICS UNCERTAIN; LETHAL']",
"term_type": "cell line"
},
{
"accession": "CLO:0024246",
"name": "GM10502 cell",
"definition": "[' CHROMOSOME 17 REGIONAL MAPPING PANEL SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
},
{
"accession": "CLO:0024247",
"name": "GM10496 cell",
"definition": "[' PYGMY POPULATION SNP500 PANEL']",
"term_type": "cell line"
},
{
"accession": "CLO:0024248",
"name": "GM10497 cell",
"definition": "[' OSTEOGENESIS IMPERFECTA: AUTOSOMAL DOMINANT- 166200,166210,166220, OR 166230']",
"term_type": "cell line"
},
{
"accession": "CLO:0024249",
"name": "GM10498 cell",
"definition": "[' NIGMS MAPPING PANEL #2, VERSION 3, HUMAN/RODENT SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
},
{
"accession": "CLO:0024250",
"name": "GM10495 cell",
"definition": "[' SNP500 PANEL PYGMY POPULATION']",
"term_type": "cell line"
},
{
"accession": "CLO:0024251",
"name": "GM10494 cell",
"definition": "[' SNP500 PANEL PYGMY POPULATION']",
"term_type": "cell line"
}
]
}