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{
"count": 43797,
"next": "https://cinder.proteo.info/api/ms_vocab/?format=api&limit=20&offset=13220&ordering=name",
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"results": [
{
"accession": "CLO:0032341",
"name": "GM01972 cell",
"definition": "[' HUTCHINSON-GILFORD PROGERIA SYNDROME; HGPS']",
"term_type": "cell line"
},
{
"accession": "CLO:0032339",
"name": "GM01981 cell",
"definition": "[' MENKES SYNDROME ATPASE, CU(2+)-TRANSPORTING, ALPHA POLYPEPTIDE; ATP7A']",
"term_type": "cell line"
},
{
"accession": "CLO:0032357",
"name": "GM01982 cell",
"definition": "[' MENKES SYNDROME ATPASE, CU(2+)-TRANSPORTING, ALPHA POLYPEPTIDE; ATP7A']",
"term_type": "cell line"
},
{
"accession": "CLO:0032358",
"name": "GM01983 cell",
"definition": "[' MENKES SYNDROME']",
"term_type": "cell line"
},
{
"accession": "CLO:0032355",
"name": "GM01984 cell",
"definition": "[' MENKES SYNDROME']",
"term_type": "cell line"
},
{
"accession": "CLO:0032356",
"name": "GM01989 cell",
"definition": "[' APPARENTLY HEALTHY NON-FETAL TISSUE']",
"term_type": "cell line"
},
{
"accession": "CLO:0032353",
"name": "GM01990 cell",
"definition": "[' APPARENTLY HEALTHY NON-FETAL TISSUE']",
"term_type": "cell line"
},
{
"accession": "CLO:0032354",
"name": "GM01993 cell",
"definition": "[' ANEUPLOID CHROMOSOME NUMBER - NON-TRISOMIC']",
"term_type": "cell line"
},
{
"accession": "CLO:0032281",
"name": "GM01995 cell",
"definition": "[' SITOSTEROLEMIA']",
"term_type": "cell line"
},
{
"accession": "CLO:0032286",
"name": "GM01996 cell",
"definition": "[' GALACTOSEMIA GALACTOSE-1-PHOSPHATE URIDYLYLTRANSFERASE; GALT']",
"term_type": "cell line"
},
{
"accession": "CLO:0032285",
"name": "GM01997 cell",
"definition": "[' ADENOSINE DEAMINASE; ADA SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE, B CELL-NEGATIVE, NK CELL-NEGATIVE, DUE TO ADENOSINE DEAMINASE DEFICIENCY']",
"term_type": "cell line"
},
{
"accession": "CLO:0032291",
"name": "GM01998 cell",
"definition": "[' TRANSTHYRETIN; TTR']",
"term_type": "cell line"
},
{
"accession": "CLO:0032288",
"name": "GM01999 cell",
"definition": "[' TRANSTHYRETIN; TTR']",
"term_type": "cell line"
},
{
"accession": "CLO:0032294",
"name": "GM02000 cell",
"definition": "[' HYPERCHOLESTEROLEMIA, FAMILIAL; FHC']",
"term_type": "cell line"
},
{
"accession": "CLO:0032295",
"name": "GM02003 cell",
"definition": "[' CHROMOSOME DELETION']",
"term_type": "cell line"
},
{
"accession": "CLO:0032296",
"name": "GM02004 cell",
"definition": "[' XERODERMA PIGMENTOSUM WITH NORMAL DNA REPAIR RATES']",
"term_type": "cell line"
},
{
"accession": "CLO:0032297",
"name": "GM02007 cell",
"definition": "[' EHLERS-DANLOS SYNDROME, TYPE I; EDS1']",
"term_type": "cell line"
},
{
"accession": "CLO:0032298",
"name": "GM02008 cell",
"definition": "[' CHROMOSOME DELETION']",
"term_type": "cell line"
},
{
"accession": "CLO:0032301",
"name": "GM02009 cell",
"definition": "[' XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP A; XPA']",
"term_type": "cell line"
},
{
"accession": "CLO:0032300",
"name": "GM02010 cell",
"definition": "[' XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP A; XPA']",
"term_type": "cell line"
}
]
}