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{
"accession": "CLO:0019526",
"name": "GM16391 cell",
"definition": "[' TRICHOTHIODYSTROPHY; TTD ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH RETARDATION, INCLUDED']",
"term_type": "cell line"
},
{
"accession": "CLO:0019389",
"name": "GM16390 cell",
"definition": "[' XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP D; XPD']",
"term_type": "cell line"
},
{
"accession": "CLO:0019385",
"name": "GM16389 cell",
"definition": "[' POPLITEAL PTERYGIUM SYNDROME, LETHAL TYPE; BARTSOCAS-PAPAS SYNDROME; BPS']",
"term_type": "cell line"
},
{
"accession": "CLO:0019394",
"name": "GM16387 cell",
"definition": "[' SOLUTE CARRIER FAMILY 3, MEMBER 1; SLC3A1 CYSTINURIA; CSNU']",
"term_type": "cell line"
},
{
"accession": "CLO:0019392",
"name": "GM16386 cell",
"definition": "[' XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC']",
"term_type": "cell line"
},
{
"accession": "CLO:0019398",
"name": "GM16385 cell",
"definition": "[' XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC']",
"term_type": "cell line"
},
{
"accession": "CLO:0019396",
"name": "GM16384 cell",
"definition": "[' XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC']",
"term_type": "cell line"
},
{
"accession": "CLO:0019400",
"name": "GM16383 cell",
"definition": "[' XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC']",
"term_type": "cell line"
},
{
"accession": "CLO:0019399",
"name": "GM16382 cell",
"definition": "[' RETT SYNDROME; RTT METHYL-CPG-BINDING PROTEIN 2; MECP2']",
"term_type": "cell line"
},
{
"accession": "CLO:0019404",
"name": "GM16381 cell",
"definition": "[' XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC']",
"term_type": "cell line"
},
{
"accession": "CLO:0019401",
"name": "GM16380 cell",
"definition": "[' XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC']",
"term_type": "cell line"
},
{
"accession": "CLO:0019415",
"name": "GM16379 cell",
"definition": "[' XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC']",
"term_type": "cell line"
},
{
"accession": "CLO:0019414",
"name": "GM16378 cell",
"definition": "[' PINEAL HYPERPLASIA, INSULIN-RESISTANT DIABETES MELLITUS, AND SOMATIC ABNORMALITIES; RABSON-MENDENHALL SYNDROME LEPRECHAUNISM']",
"term_type": "cell line"
},
{
"accession": "CLO:0019411",
"name": "GM16377 cell",
"definition": "[' BLOOM SYNDROME; BLM RECQ PROTEIN-LIKE 3; RECQL3']",
"term_type": "cell line"
},
{
"accession": "CLO:0019421",
"name": "GM16375 cell",
"definition": "[' RECQ PROTEIN-LIKE 3; RECQL3 BLOOM SYNDROME; BLM']",
"term_type": "cell line"
},
{
"accession": "CLO:0019420",
"name": "GM16372 cell",
"definition": "[' HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME; HRD; SANJAD-SAKATI SYNDROME']",
"term_type": "cell line"
},
{
"accession": "CLO:0019419",
"name": "GM16370 cell",
"definition": "[' XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC']",
"term_type": "cell line"
},
{
"accession": "CLO:0019418",
"name": "GM16368 cell",
"definition": "[' RETT SYNDROME; RTT METHYL-CPG-BINDING PROTEIN 2; MECP2']",
"term_type": "cell line"
},
{
"accession": "CLO:0019425",
"name": "GM16352 cell",
"definition": "[' FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY; TYPE UNKNOWN (FSHD)']",
"term_type": "cell line"
},
{
"accession": "CLO:0019424",
"name": "GM16351 cell",
"definition": "[' FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY; TYPE UNKNOWN (FSHD)']",
"term_type": "cell line"
}
]
}