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{
"count": 43797,
"next": "https://cinder.proteo.info/api/ms_vocab/?format=api&limit=20&offset=24260&ordering=-accession",
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"results": [
{
"accession": "CLO:0018768",
"name": "GM12103 cell",
"definition": "[' CEPH/UTAH PEDIGREE 1413']",
"term_type": "cell line"
},
{
"accession": "CLO:0018767",
"name": "AG15111 cell",
"definition": "[' APPARENTLY HEALTHY NON-FETAL TISSUE']",
"term_type": "cell line"
},
{
"accession": "CLO:0018766",
"name": "AG15173 cell",
"definition": "[' APPARENTLY HEALTHY NON-FETAL TISSUE']",
"term_type": "cell line"
},
{
"accession": "CLO:0018765",
"name": "GM12102 cell",
"definition": "[' CEPH/UTAH PEDIGREE 1413']",
"term_type": "cell line"
},
{
"accession": "CLO:0018764",
"name": "GM12101 cell",
"definition": "[' CEPH/UTAH PEDIGREE 1413']",
"term_type": "cell line"
},
{
"accession": "CLO:0018763",
"name": "GM12100 cell",
"definition": "[' CEPH/UTAH PEDIGREE 1332']",
"term_type": "cell line"
},
{
"accession": "CLO:0018762",
"name": "GM16024 cell",
"definition": "[' XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP G; XPG']",
"term_type": "cell line"
},
{
"accession": "CLO:0018761",
"name": "ND06633 cell",
"definition": "[' EPILEPSY']",
"term_type": "cell line"
},
{
"accession": "CLO:0018760",
"name": "GM16028 cell",
"definition": "[' HUMAN GENE MUTATION PANEL - HEMOCHROMATOSIS 5,10-@METHYLENETETRAHYDROFOLATE REDUCTASE; MTHFR FACTOR V DEFICIENCY HUMAN GENE MUTATION PANEL - DISORDERS OF THROMBOSIS COAGULATION FACTOR II; F2 HEMOCHROMATOSIS; HFE']",
"term_type": "cell line"
},
{
"accession": "CLO:0018759",
"name": "GM16027 cell",
"definition": "[' DERIVATIVE CHROMOSOME TRANSLOCATED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0018758",
"name": "GM16081 cell",
"definition": "[' PALMITOYL-PROTEIN THIOESTERASE 1; PPT1 CEROID LIPOFUSCINOSIS, JUVENILE NEURONAL, WITH GRANULAR OSMIOPHILIC DEPOSIT']",
"term_type": "cell line"
},
{
"accession": "CLO:0018757",
"name": "GM16080 cell",
"definition": "[' PALMITOYL-PROTEIN THIOESTERASE 1; PPT1 CEROID LIPOFUSCINOSIS, JUVENILE NEURONAL, WITH GRANULAR OSMIOPHILIC DEPOSIT']",
"term_type": "cell line"
},
{
"accession": "CLO:0018756",
"name": "AG15059 cell",
"definition": "[' APPARENTLY HEALTHY NON-FETAL TISSUE']",
"term_type": "cell line"
},
{
"accession": "CLO:0018755",
"name": "GM16083 cell",
"definition": "[' CEROID LIPOFUSCINOSIS, NEURONAL 1, INFANTILE; CLN1 PALMITOYL-PROTEIN THIOESTERASE 1; PPT1']",
"term_type": "cell line"
},
{
"accession": "CLO:0018754",
"name": "AG15060 cell",
"definition": "[' APPARENTLY HEALTHY NON-FETAL TISSUE']",
"term_type": "cell line"
},
{
"accession": "CLO:0018753",
"name": "GM16082 cell",
"definition": "[' CEROID LIPOFUSCINOSIS, NEURONAL 1, INFANTILE; CLN1 PALMITOYL-PROTEIN THIOESTERASE 1; PPT1']",
"term_type": "cell line"
},
{
"accession": "CLO:0018752",
"name": "AG15090 cell",
"definition": "[' APPARENTLY HEALTHY NON-FETAL TISSUE']",
"term_type": "cell line"
},
{
"accession": "CLO:0018751",
"name": "ND06639 cell",
"definition": "[\" PARKINSON'S DISEASE\"]",
"term_type": "cell line"
},
{
"accession": "CLO:0018750",
"name": "ND06640 cell",
"definition": "[\" PARKINSON'S DISEASE\"]",
"term_type": "cell line"
},
{
"accession": "CLO:0018749",
"name": "ND06663 cell",
"definition": "[' EPILEPSY']",
"term_type": "cell line"
}
]
}