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{
"count": 43797,
"next": "https://cinder.proteo.info/api/ms_vocab/?format=api&limit=20&offset=19880&ordering=-accession",
"previous": "https://cinder.proteo.info/api/ms_vocab/?format=api&limit=20&offset=19840&ordering=-accession",
"results": [
{
"accession": "CLO:0023148",
"name": "DA05909 cell",
"definition": "[' DIABETES MELLITUS FAMILY SAMPLE']",
"term_type": "cell line"
},
{
"accession": "CLO:0023147",
"name": "GM06214 cell",
"definition": "[' HURLER SYNDROME ALPHA-L-IDURONIDASE; IDUA']",
"term_type": "cell line"
},
{
"accession": "CLO:0023146",
"name": "GM06221 cell",
"definition": "[' PROTOPORPHYRIA, ERYTHROPOIETIC']",
"term_type": "cell line"
},
{
"accession": "CLO:0023145",
"name": "GM06222 cell",
"definition": "[' CHROMOSOME DELETION']",
"term_type": "cell line"
},
{
"accession": "CLO:0023144",
"name": "GM06224 cell",
"definition": "[' KEARNS-SAYRE SYNDROME; KSS']",
"term_type": "cell line"
},
{
"accession": "CLO:0023143",
"name": "GM06225 cell",
"definition": "[' KEARNS-SAYRE SYNDROME; KSS']",
"term_type": "cell line"
},
{
"accession": "CLO:0023142",
"name": "GM06199 cell",
"definition": "[' RING CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0023141",
"name": "GM06197 cell",
"definition": "[' BARDET-BIEDL SYNDROME, BBS']",
"term_type": "cell line"
},
{
"accession": "CLO:0023140",
"name": "GM06201 cell",
"definition": "[' SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE, B CELL-NEGATIVE, NK CELL-NEGATIVE, DUE TO ADENOSINE DEAMINASE DEFICIENCY ADENOSINE DEAMINASE; ADA']",
"term_type": "cell line"
},
{
"accession": "CLO:0023139",
"name": "GM06200 cell",
"definition": "[' SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE, B CELL-NEGATIVE, NK CELL-NEGATIVE, DUE TO ADENOSINE DEAMINASE DEFICIENCY ADENOSINE DEAMINASE; ADA']",
"term_type": "cell line"
},
{
"accession": "CLO:0023138",
"name": "GM06207 cell",
"definition": "[' FELIS']",
"term_type": "cell line"
},
{
"accession": "CLO:0023137",
"name": "GM06206 cell",
"definition": "[' FELINE EHLERS-DANLOS SYNDROME: TYPE UNCLASSIFIED FELIS']",
"term_type": "cell line"
},
{
"accession": "CLO:0023136",
"name": "GM06195 cell",
"definition": "[' BARDET-BIEDL SYNDROME, BBS']",
"term_type": "cell line"
},
{
"accession": "CLO:0023135",
"name": "GM06196 cell",
"definition": "[' BARDET-BIEDL SYNDROME, BBS']",
"term_type": "cell line"
},
{
"accession": "CLO:0023134",
"name": "GM06188 cell",
"definition": "[' TUBEROUS SCLEROSIS; TS TSC2 GENE; TSC2']",
"term_type": "cell line"
},
{
"accession": "CLO:0023133",
"name": "GM06194 cell",
"definition": "[' TUBEROUS SCLEROSIS; TS']",
"term_type": "cell line"
},
{
"accession": "CLO:0023132",
"name": "GM06318 cell",
"definition": "[' NIGMS MAPPING PANEL #2, VERSION 3, HUMAN/RODENT SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
},
{
"accession": "CLO:0023131",
"name": "GM06317 cell",
"definition": "[' NIGMS MAPPING PANEL #2, VERSION 3, HUMAN/RODENT SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
},
{
"accession": "CLO:0023130",
"name": "GM06324 cell",
"definition": "[' NEUROAXONAL DYSTROPHY, INFANTILE']",
"term_type": "cell line"
},
{
"accession": "CLO:0023129",
"name": "GM06321 cell",
"definition": "[' TRANSLOCATED CHROMOSOME']",
"term_type": "cell line"
}
]
}