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{
"accession": "CLO:0029555",
"name": "GM20382 cell",
"definition": "[' CEROID LIPOFUSCINOSIS, NEURONAL 3, JUVENILE; CLN3 CLN3 GENE; CLN3']",
"term_type": "cell line"
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{
"accession": "CLO:0029554",
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"definition": "[' CEROID LIPOFUSCINOSIS, NEURONAL 3, JUVENILE; CLN3 CLN3 GENE; CLN3']",
"term_type": "cell line"
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{
"accession": "CLO:0029553",
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"definition": "[' CEROID LIPOFUSCINOSIS, NEURONAL 3, JUVENILE; CLN3 CLN3 GENE; CLN3']",
"term_type": "cell line"
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{
"accession": "CLO:0029551",
"name": "GM20385 cell",
"definition": "[' CEROID LIPOFUSCINOSIS, NEURONAL 2, LATE INFANTILE TYPE; CLN2 CLN2 GENE; CLN2']",
"term_type": "cell line"
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{
"accession": "CLO:0029548",
"name": "GM20387 cell",
"definition": "[' CEROID LIPOFUSCINOSIS, NEURONAL 2, LATE INFANTILE TYPE; CLN2 CLN2 GENE; CLN2']",
"term_type": "cell line"
},
{
"accession": "CLO:0029547",
"name": "GM20389 cell",
"definition": "[' CEROID LIPOFUSCINOSIS, NEURONAL 1, INFANTILE; CLN1 PALMITOYL-PROTEIN THIOESTERASE 1; PPT1']",
"term_type": "cell line"
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{
"accession": "CLO:0029577",
"name": "GM20390 cell",
"definition": "[' TRANSLOCATED CHROMOSOME ACUTE LYMPHOCYTIC LEUKEMIA']",
"term_type": "cell line"
},
{
"accession": "CLO:0029579",
"name": "GM20392 cell",
"definition": "[' HYPOXANTHINE GUANINE PHOSPHORIBOSYLTRANSFERASE 1; HPRT1; HPRT LESCH-NYHAN SYNDROME; LNS']",
"term_type": "cell line"
},
{
"accession": "CLO:0029578",
"name": "GM20393 cell",
"definition": "[' LESCH-NYHAN SYNDROME; LNS HYPOXANTHINE GUANINE PHOSPHORIBOSYLTRANSFERASE 1; HPRT1; HPRT']",
"term_type": "cell line"
},
{
"accession": "CLO:0029574",
"name": "GM20394 cell",
"definition": "[' LESCH-NYHAN SYNDROME; LNS HYPOXANTHINE GUANINE PHOSPHORIBOSYLTRANSFERASE 1; HPRT1; HPRT']",
"term_type": "cell line"
},
{
"accession": "CLO:0029573",
"name": "GM20395 cell",
"definition": "[' LESCH-NYHAN SYNDROME; LNS HYPOXANTHINE GUANINE PHOSPHORIBOSYLTRANSFERASE 1; HPRT1; HPRT']",
"term_type": "cell line"
},
{
"accession": "CLO:0029576",
"name": "GM20396 cell",
"definition": "[' LESCH-NYHAN SYNDROME; LNS HYPOXANTHINE GUANINE PHOSPHORIBOSYLTRANSFERASE 1; HPRT1; HPRT']",
"term_type": "cell line"
},
{
"accession": "CLO:0029575",
"name": "GM20397 cell",
"definition": "[' LESCH-NYHAN SYNDROME; LNS HYPOXANTHINE GUANINE PHOSPHORIBOSYLTRANSFERASE 1; HPRT1; HPRT']",
"term_type": "cell line"
},
{
"accession": "CLO:0029569",
"name": "GM20398 cell",
"definition": "[' LESCH-NYHAN SYNDROME; LNS HYPOXANTHINE GUANINE PHOSPHORIBOSYLTRANSFERASE 1; HPRT1; HPRT']",
"term_type": "cell line"
},
{
"accession": "CLO:0029566",
"name": "GM20399 cell",
"definition": "[' ALPERS DIFFUSE DEGENERATION OF CEREBRAL GRAY MATTER WITH HEPATIC CIRRHOSIS POLYMERASE, DNA, GAMMA; POLG']",
"term_type": "cell line"
},
{
"accession": "CLO:0029572",
"name": "GM20400 cell",
"definition": "[' POLYMERASE, DNA, GAMMA; POLG ALPERS DIFFUSE DEGENERATION OF CEREBRAL GRAY MATTER WITH HEPATIC CIRRHOSIS']",
"term_type": "cell line"
},
{
"accession": "CLO:0029518",
"name": "GM20406 cell",
"definition": "[' PRADER-WILLI SYNDROME; PWS CHROMOSOME DELETION']",
"term_type": "cell line"
},
{
"accession": "CLO:0029517",
"name": "GM20408 cell",
"definition": "[' PRADER-WILLI SYNDROME; PWS COMPLETE MATERNAL UNIPARENTAL DISOMY']",
"term_type": "cell line"
},
{
"accession": "CLO:0029516",
"name": "GM20409 cell",
"definition": "[' ANGELMAN SYNDROME; AS COMPLETE PATERNAL UNIPARENTAL DISOMY']",
"term_type": "cell line"
},
{
"accession": "CLO:0029515",
"name": "GM20410 cell",
"definition": "[' CHROMOSOME DELETION ANGELMAN SYNDROME; AS']",
"term_type": "cell line"
}
]
}