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{
"count": 43797,
"next": "https://cinder.proteo.info/api/ms_vocab/?format=api&limit=20&offset=22560&ordering=-name",
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"results": [
{
"accession": "CLO:0016185",
"name": "GM17897 cell",
"definition": "[' CLEIDOCRANIAL DYSPLASIA; CCD']",
"term_type": "cell line"
},
{
"accession": "CLO:0016195",
"name": "GM17896 cell",
"definition": "[' CLEIDOCRANIAL DYSPLASIA; CCD']",
"term_type": "cell line"
},
{
"accession": "CLO:0016149",
"name": "GM17895 cell",
"definition": "[' FRONTONASAL DYSPLASIA']",
"term_type": "cell line"
},
{
"accession": "CLO:0016147",
"name": "GM17894 cell",
"definition": "[' NORMAL CHROMOSOMAL POLYMORPHISM APPARENTLY HEALTHY NON-FETAL TISSUE']",
"term_type": "cell line"
},
{
"accession": "CLO:0016151",
"name": "GM17890 cell",
"definition": "[' ADAPTOR-RELATED PROTEIN COMPLEX 3, BETA-1 SUBUNIT; AP3B1 HERMANSKY-PUDLAK SYNDROME 2; HPS2']",
"term_type": "cell line"
},
{
"accession": "CLO:0016150",
"name": "GM17888 cell",
"definition": "[' CYSTINOSIS, ADULT NONNEPHROPATHIC CYSTINOSIN; CTNS']",
"term_type": "cell line"
},
{
"accession": "CLO:0016142",
"name": "GM17886 cell",
"definition": "[' CYSTINOSIS, NEPHROPATHIC; CTNS CYSTINOSIN; CTNS']",
"term_type": "cell line"
},
{
"accession": "CLO:0016139",
"name": "GM17885 cell",
"definition": "[' CYSTINOSIN; CTNS CYSTINOSIS, NEPHROPATHIC; CTNS']",
"term_type": "cell line"
},
{
"accession": "CLO:0016145",
"name": "GM17883 cell",
"definition": "[' XXY SYNDROME; KLINEFELTER SYNDROME ANEUPLOID CHROMOSOME NUMBER - NON-TRISOMIC']",
"term_type": "cell line"
},
{
"accession": "CLO:0016143",
"name": "GM17881 cell",
"definition": "[' HERMANSKY-PUDLAK SYNDROME; HPS HERMANSKY-PUDLAK SYNDROME GENE 6']",
"term_type": "cell line"
},
{
"accession": "CLO:0016152",
"name": "GM17880 cell",
"definition": "[' METHYL-CPG-BINDING PROTEIN 2; MECP2 RETT SYNDROME; RTT']",
"term_type": "cell line"
},
{
"accession": "CLO:0016459",
"name": "GM17879 cell",
"definition": "[' ANEUPLOID CHROMOSOME NUMBER - NON-TRISOMIC XXY SYNDROME; KLINEFELTER SYNDROME']",
"term_type": "cell line"
},
{
"accession": "CLO:0016460",
"name": "GM17869 cell",
"definition": "[' FSHD GENE 1; FRG1 FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1A; FSHMD1A (FSHD)']",
"term_type": "cell line"
},
{
"accession": "CLO:0016461",
"name": "GM17868 cell",
"definition": "[' FSHD GENE 1; FRG1 FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1A; FSHMD1A (FSHD)']",
"term_type": "cell line"
},
{
"accession": "CLO:0016462",
"name": "GM17867 cell",
"definition": "[' ANEUPLOID CHROMOSOME NUMBER - NON-TRISOMIC XXY SYNDROME; KLINEFELTER SYNDROME']",
"term_type": "cell line"
},
{
"accession": "CLO:0016463",
"name": "GM17861 cell",
"definition": "[' XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC']",
"term_type": "cell line"
},
{
"accession": "CLO:0016464",
"name": "GM17860 cell",
"definition": "[' XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC']",
"term_type": "cell line"
},
{
"accession": "CLO:0016465",
"name": "GM17858 cell",
"definition": "[' XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC']",
"term_type": "cell line"
},
{
"accession": "CLO:0016467",
"name": "GM17857 cell",
"definition": "[' ANEUPLOID CHROMOSOME NUMBER - NON-TRISOMIC XXY SYNDROME; KLINEFELTER SYNDROME']",
"term_type": "cell line"
},
{
"accession": "CLO:0016466",
"name": "GM17856 cell",
"definition": "[' HUMAN VARIATION PANEL - HAN PEOPLE OF LOS ANGELES PANEL OF 100']",
"term_type": "cell line"
}
]
}