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{
"count": 43797,
"next": "https://cinder.proteo.info/api/ms_vocab/?format=api&limit=20&offset=27060&ordering=-name",
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"results": [
{
"accession": "CLO:0029743",
"name": "GM09947 cell",
"definition": "[' APPARENTLY HEALTHY NON-FETAL TISSUE']",
"term_type": "cell line"
},
{
"accession": "CLO:0029741",
"name": "GM09946 cell",
"definition": "[' CHROMOSOME DELETION']",
"term_type": "cell line"
},
{
"accession": "CLO:0029755",
"name": "GM09944 cell",
"definition": "[' NEUROFIBROMATOSIS, TYPE I; NF1']",
"term_type": "cell line"
},
{
"accession": "CLO:0029754",
"name": "GM09943 cell",
"definition": "[' XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC']",
"term_type": "cell line"
},
{
"accession": "CLO:0029757",
"name": "GM09942 cell",
"definition": "[' XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC']",
"term_type": "cell line"
},
{
"accession": "CLO:0029756",
"name": "GM09923 cell",
"definition": "[' APPARENTLY HEALTHY NON-FETAL TISSUE']",
"term_type": "cell line"
},
{
"accession": "CLO:0029759",
"name": "GM09922 cell",
"definition": "[' CHROMOSOME DELETION']",
"term_type": "cell line"
},
{
"accession": "CLO:0029758",
"name": "GM09919 cell",
"definition": "[' HYPOPHOSPHATASIA; PHOSPHOETHANOLAMINURIA - 241500 OR 241510']",
"term_type": "cell line"
},
{
"accession": "CLO:0029761",
"name": "GM09918 cell",
"definition": "[' APPARENTLY HEALTHY NON-FETAL TISSUE']",
"term_type": "cell line"
},
{
"accession": "CLO:0029760",
"name": "GM09913 cell",
"definition": "[' GIANT CELL HEPATITIS, NEONATAL IDIOPATHIC NEONATAL HEMOCHROMATOSIS, INCLUDED']",
"term_type": "cell line"
},
{
"accession": "CLO:0029763",
"name": "GM09912 cell",
"definition": "[' GIANT CELL HEPATITIS, NEONATAL IDIOPATHIC NEONATAL HEMOCHROMATOSIS, INCLUDED']",
"term_type": "cell line"
},
{
"accession": "CLO:0029762",
"name": "GM09911 cell",
"definition": "[' GILLES DE LA TOURETTE SYNDROME; GTS']",
"term_type": "cell line"
},
{
"accession": "CLO:0030561",
"name": "GM09910 cell",
"definition": "[' NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE III; HSAN3']",
"term_type": "cell line"
},
{
"accession": "CLO:0030560",
"name": "GM09909 cell",
"definition": "[' NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE III; HSAN3']",
"term_type": "cell line"
},
{
"accession": "CLO:0030552",
"name": "GM09901 cell",
"definition": "[' EPIDERMOLYSIS BULLOSA: DYSTROPHIC, JUNCTIONAL, OR SIMPLEX TYPES']",
"term_type": "cell line"
},
{
"accession": "CLO:0030550",
"name": "GM09899 cell",
"definition": "[' APPARENTLY HEALTHY NON-FETAL TISSUE']",
"term_type": "cell line"
},
{
"accession": "CLO:0030556",
"name": "GM09894 cell",
"definition": "[' GIANT CELL HEPATITIS, NEONATAL IDIOPATHIC NEONATAL HEMOCHROMATOSIS, INCLUDED']",
"term_type": "cell line"
},
{
"accession": "CLO:0030553",
"name": "GM09893 cell",
"definition": "[' GIANT CELL HEPATITIS, NEONATAL IDIOPATHIC NEONATAL HEMOCHROMATOSIS, INCLUDED']",
"term_type": "cell line"
},
{
"accession": "CLO:0030580",
"name": "GM09892 cell",
"definition": "[' CHROMOSOME DELETION']",
"term_type": "cell line"
},
{
"accession": "CLO:0030582",
"name": "GM09888 cell",
"definition": "[' CHROMOSOME DELETION TRICHORHINOPHALANGEAL SYNDROME, TYPE II; TRPS2 (LANGER-GIEDION SYNDROME; LGS)']",
"term_type": "cell line"
}
]
}