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{
"accession": "CLO:0017587",
"name": "GM16523 cell",
"definition": "[' ADRENOLEUKODYSTROPHY, AUTOSOMAL NEONATAL FORM']",
"term_type": "cell line"
},
{
"accession": "CLO:0017488",
"name": "GM16521 cell",
"definition": "[' ADRENOLEUKODYSTROPHY, AUTOSOMAL NEONATAL FORM']",
"term_type": "cell line"
},
{
"accession": "CLO:0017489",
"name": "GM16514 cell",
"definition": "[' ZELLWEGER SYNDROME; ZS']",
"term_type": "cell line"
},
{
"accession": "CLO:0017490",
"name": "GM16513 cell",
"definition": "[' PEROXISOME BIOGENESIS FACTOR 1; PEX1 ZELLWEGER SYNDROME; ZS']",
"term_type": "cell line"
},
{
"accession": "CLO:0017482",
"name": "GM16512 cell",
"definition": "[' ADRENOLEUKODYSTROPHY, AUTOSOMAL NEONATAL FORM']",
"term_type": "cell line"
},
{
"accession": "CLO:0017483",
"name": "GM16510 cell",
"definition": "[' ADRENOLEUKODYSTROPHY, AUTOSOMAL NEONATAL FORM']",
"term_type": "cell line"
},
{
"accession": "CLO:0017485",
"name": "GM16500 cell",
"definition": "[' CYSTINURIA; CSNU SOLUTE CARRIER FAMILY 3, MEMBER 1; SLC3A1']",
"term_type": "cell line"
},
{
"accession": "CLO:0017487",
"name": "GM16499 cell",
"definition": "[' CLEFT HAND AND ABSENT TIBIA']",
"term_type": "cell line"
},
{
"accession": "CLO:0017491",
"name": "GM16497 cell",
"definition": "[' METHYL-CPG-BINDING PROTEIN 2; MECP2 RETT SYNDROME; RTT']",
"term_type": "cell line"
},
{
"accession": "CLO:0017492",
"name": "GM16495 cell",
"definition": "[' ZELLWEGER SYNDROME; ZS']",
"term_type": "cell line"
},
{
"accession": "CLO:0017493",
"name": "GM16494 cell",
"definition": "[' REFSUM DISEASE, INFANTILE FORM']",
"term_type": "cell line"
},
{
"accession": "CLO:0017521",
"name": "GM16493 cell",
"definition": "[' REFSUM DISEASE, INFANTILE FORM']",
"term_type": "cell line"
},
{
"accession": "CLO:0017522",
"name": "GM16492 cell",
"definition": "[' RETINITIS PIGMENTOSA 1; RP1 REFSUM DISEASE']",
"term_type": "cell line"
},
{
"accession": "CLO:0017519",
"name": "GM16491 cell",
"definition": "[' RETINITIS PIGMENTOSA 1; RP1 REFSUM DISEASE']",
"term_type": "cell line"
},
{
"accession": "CLO:0017520",
"name": "GM16490 cell",
"definition": "[' ADDITIONAL DELETION/DERIVATIVE CHROMOSOME 18 SOMATIC CELL HYBRIDS ADDITIONAL DELETION/DERIVATIVE CHROMOSOME 4 SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
},
{
"accession": "CLO:0017517",
"name": "GM16486 cell",
"definition": "[' CEROID LIPOFUSCINOSIS, NEURONAL 2, LATE INFANTILE TYPE; CLN2 CLN2 GENE; CLN2']",
"term_type": "cell line"
},
{
"accession": "CLO:0017518",
"name": "GM16485 cell",
"definition": "[' CEROID LIPOFUSCINOSIS, NEURONAL 2, LATE INFANTILE TYPE; CLN2 CLN2 GENE; CLN2']",
"term_type": "cell line"
},
{
"accession": "CLO:0017513",
"name": "GM16483 cell",
"definition": "[' SOLUTE CARRIER FAMILY 3, MEMBER 1; SLC3A1 CYSTINURIA; CSNU']",
"term_type": "cell line"
},
{
"accession": "CLO:0017515",
"name": "GM16482 cell",
"definition": "[' CYSTINURIA; CSNU SOLUTE CARRIER FAMILY 3, MEMBER 1; SLC3A1']",
"term_type": "cell line"
},
{
"accession": "CLO:0017523",
"name": "GM16481 cell",
"definition": "[' CYSTINURIA; CSNU SOLUTE CARRIER FAMILY 3, MEMBER 1; SLC3A1']",
"term_type": "cell line"
}
]
}