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{
"count": 43797,
"next": "https://cinder.proteo.info/api/ms_vocab/?format=api&limit=20&offset=13280&ordering=name",
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"results": [
{
"accession": "CLO:0032518",
"name": "GM02068 cell",
"definition": "[' TRANSLOCATED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0032512",
"name": "GM02074 cell",
"definition": "[' MUCOPOLYSACCHARIDOSIS TYPE VII']",
"term_type": "cell line"
},
{
"accession": "CLO:0032513",
"name": "GM02075 cell",
"definition": "[' CHEDIAK-HIGASHI SYNDROME; CHS1 LYSOSOMAL TRAFFICKING REGULATOR, INCLUDED; LYST, INCLUDED']",
"term_type": "cell line"
},
{
"accession": "CLO:0032514",
"name": "GM02077 cell",
"definition": "[' HUNTINGTON DISEASE; HD']",
"term_type": "cell line"
},
{
"accession": "CLO:0032515",
"name": "GM02078 cell",
"definition": "[' HUNTINGTON DISEASE; HD']",
"term_type": "cell line"
},
{
"accession": "CLO:0032509",
"name": "GM02079 cell",
"definition": "[' HUNTINGTON DISEASE; HD']",
"term_type": "cell line"
},
{
"accession": "CLO:0032510",
"name": "GM02080 cell",
"definition": "[' HUNTINGTON DISEASE; HD']",
"term_type": "cell line"
},
{
"accession": "CLO:0032511",
"name": "GM02085 cell",
"definition": "[' RECQ PROTEIN-LIKE 3; RECQL3 BLOOM SYNDROME; BLM']",
"term_type": "cell line"
},
{
"accession": "CLO:0031826",
"name": "GM02090 cell",
"definition": "[' XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP A; XPA']",
"term_type": "cell line"
},
{
"accession": "CLO:0031825",
"name": "GM02091 cell",
"definition": "[' XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP A; XPA']",
"term_type": "cell line"
},
{
"accession": "CLO:0031828",
"name": "GM02093 cell",
"definition": "[' METACHROMATIC LEUKODYSTROPHY, LATE-INFANTILE']",
"term_type": "cell line"
},
{
"accession": "CLO:0031827",
"name": "GM02094 cell",
"definition": "[' SANDHOFF DISEASE']",
"term_type": "cell line"
},
{
"accession": "CLO:0031822",
"name": "GM02095 cell",
"definition": "[' METACHROMATIC LEUKODYSTROPHY, LATE-INFANTILE']",
"term_type": "cell line"
},
{
"accession": "CLO:0031821",
"name": "GM02096 cell",
"definition": "[' XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC']",
"term_type": "cell line"
},
{
"accession": "CLO:0031824",
"name": "GM02098 cell",
"definition": "[' BASAL CELL NEVUS SYNDROME; BCNS']",
"term_type": "cell line"
},
{
"accession": "CLO:0031823",
"name": "GM02099 cell",
"definition": "[' BASAL CELL NEVUS SYNDROME; BCNS']",
"term_type": "cell line"
},
{
"accession": "CLO:0031820",
"name": "GM02103 cell",
"definition": "[' TRANSLOCATED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0031819",
"name": "GM02109 cell",
"definition": "[' WOLMAN DISEASE']",
"term_type": "cell line"
},
{
"accession": "CLO:0031830",
"name": "GM02110 cell",
"definition": "[' HYPERCHOLESTEROLEMIA, FAMILIAL; FHC']",
"term_type": "cell line"
},
{
"accession": "CLO:0031848",
"name": "GM02123 cell",
"definition": "[' HUNTINGTON DISEASE; HD']",
"term_type": "cell line"
}
]
}