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{
"count": 43797,
"next": "https://cinder.proteo.info/api/ms_vocab/?format=api&limit=20&offset=18880&ordering=accession",
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"results": [
{
"accession": "CLO:0018072",
"name": "GM16957 cell",
"definition": "[' XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP D; XPD']",
"term_type": "cell line"
},
{
"accession": "CLO:0018073",
"name": "GM16956 cell",
"definition": "[' XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP D; XPD']",
"term_type": "cell line"
},
{
"accession": "CLO:0018074",
"name": "GM16964 cell",
"definition": "[' OSTEOGENESIS IMPERFECTA, TYPE IV; OI4 COLLAGEN, TYPE I, ALPHA-2; COL1A2']",
"term_type": "cell line"
},
{
"accession": "CLO:0018075",
"name": "GM16963 cell",
"definition": "[' OSTEOGENESIS IMPERFECTA, TYPE IV; OI4 COLLAGEN, TYPE I, ALPHA-2; COL1A2']",
"term_type": "cell line"
},
{
"accession": "CLO:0018076",
"name": "GM16955 cell",
"definition": "[' XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP D; XPD']",
"term_type": "cell line"
},
{
"accession": "CLO:0018077",
"name": "GM12604 cell",
"definition": "[' ORNITHINE CARBAMOYLTRANSFERASE; OTC ORNITHINE TRANSCARBAMYLASE DEFICIENCY, HYPERAMMONEMIA DUE TO; OTC']",
"term_type": "cell line"
},
{
"accession": "CLO:0018078",
"name": "GM16969 cell",
"definition": "[' OSTEOGENESIS IMPERFECTA, TYPE IV; OI4 COLLAGEN, TYPE I, ALPHA-2; COL1A2']",
"term_type": "cell line"
},
{
"accession": "CLO:0018079",
"name": "GM12601 cell",
"definition": "[' HYPOPLASTIC LEFT HEART SYNDROME']",
"term_type": "cell line"
},
{
"accession": "CLO:0018080",
"name": "GM12593 cell",
"definition": "[' APPARENTLY HEALTHY NON-FETAL TISSUE']",
"term_type": "cell line"
},
{
"accession": "CLO:0018081",
"name": "GM12610 cell",
"definition": "[' RETICULOSIS, FAMILIAL HISTIOCYTIC']",
"term_type": "cell line"
},
{
"accession": "CLO:0018082",
"name": "GM16966 cell",
"definition": "[' OSTEOGENESIS IMPERFECTA, TYPE IV; OI4 COLLAGEN, TYPE I, ALPHA-2; COL1A2']",
"term_type": "cell line"
},
{
"accession": "CLO:0018083",
"name": "GM16965 cell",
"definition": "[' OSTEOGENESIS IMPERFECTA, TYPE IV; OI4 COLLAGEN, TYPE I, ALPHA-2; COL1A2']",
"term_type": "cell line"
},
{
"accession": "CLO:0018084",
"name": "GM12609 cell",
"definition": "[' POLYCYSTIC KIDNEY AND HEPATIC DISEASE 1; PKHD1']",
"term_type": "cell line"
},
{
"accession": "CLO:0018085",
"name": "GM16968 cell",
"definition": "[' OSTEOGENESIS IMPERFECTA, TYPE IV; OI4 COLLAGEN, TYPE I, ALPHA-2; COL1A2']",
"term_type": "cell line"
},
{
"accession": "CLO:0018086",
"name": "GM12607 cell",
"definition": "[' POLYCYSTIC KIDNEY AND HEPATIC DISEASE 1; PKHD1']",
"term_type": "cell line"
},
{
"accession": "CLO:0018087",
"name": "GM16967 cell",
"definition": "[' OSTEOGENESIS IMPERFECTA, TYPE IV; OI4 COLLAGEN, TYPE I, ALPHA-2; COL1A2']",
"term_type": "cell line"
},
{
"accession": "CLO:0018088",
"name": "GM12606 cell",
"definition": "[' ANEUPLOID CHROMOSOME NUMBER - NON-TRISOMIC CHROMOSOME DELETION']",
"term_type": "cell line"
},
{
"accession": "CLO:0018089",
"name": "ND06940 cell",
"definition": "[\" PARKINSON'S DISEASE\"]",
"term_type": "cell line"
},
{
"accession": "CLO:0018090",
"name": "GM12585 cell",
"definition": "[' CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; CFTR HUMAN GENE MUTATION PANEL - CYSTIC FIBROSIS (VERSION 2) CYSTIC FIBROSIS; CF']",
"term_type": "cell line"
},
{
"accession": "CLO:0018091",
"name": "ND06941 cell",
"definition": "[\" PARKINSON'S DISEASE\"]",
"term_type": "cell line"
}
]
}