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{
"count": 43797,
"next": "https://cinder.proteo.info/api/ms_vocab/?format=api&limit=20&offset=26740&ordering=-accession",
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"results": [
{
"accession": "CLO:0016288",
"name": "GM17944 cell",
"definition": "[' COLLAGEN, TYPE I, ALPHA-2; COL1A2 OSTEOGENESIS IMPERFECTA, TYPE IV; OI4']",
"term_type": "cell line"
},
{
"accession": "CLO:0016287",
"name": "GM17945 cell",
"definition": "[' OSTEOGENESIS IMPERFECTA, TYPE IV; OI4']",
"term_type": "cell line"
},
{
"accession": "CLO:0016286",
"name": "GM17940 cell",
"definition": "[' FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1A; FSHMD1A (FSHD) FSHD GENE 1; FRG1']",
"term_type": "cell line"
},
{
"accession": "CLO:0016285",
"name": "GM17942 cell",
"definition": "[' DIGEORGE SYNDROME; DGS']",
"term_type": "cell line"
},
{
"accession": "CLO:0016284",
"name": "GM17947 cell",
"definition": "[' COLLAGEN, TYPE I, ALPHA-2; COL1A2 OSTEOGENESIS IMPERFECTA, TYPE IV; OI4']",
"term_type": "cell line"
},
{
"accession": "CLO:0016283",
"name": "GM17948 cell",
"definition": "[' OSTEOGENESIS IMPERFECTA, TYPE IV; OI4 COLLAGEN, TYPE I, ALPHA-2; COL1A2']",
"term_type": "cell line"
},
{
"accession": "CLO:0016282",
"name": "GM17938 cell",
"definition": "[' VELOCARDIOFACIAL SYNDROME']",
"term_type": "cell line"
},
{
"accession": "CLO:0016281",
"name": "GM17939 cell",
"definition": "[' FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1A; FSHMD1A (FSHD) FSHD GENE 1; FRG1']",
"term_type": "cell line"
},
{
"accession": "CLO:0016280",
"name": "GM17933 cell",
"definition": "[' CHROMOSOME DELETION']",
"term_type": "cell line"
},
{
"accession": "CLO:0016279",
"name": "GM17934 cell",
"definition": "[' ANKYLOBLEPHARON-ECTODERMAL DEFECTS-CLEFT LIP/PALATE']",
"term_type": "cell line"
},
{
"accession": "CLO:0016278",
"name": "GM17921 cell",
"definition": "[' NIEMANN-PICK DISEASE, TYPE C1; NPC1 NPC1 GENE; NPC1']",
"term_type": "cell line"
},
{
"accession": "CLO:0016277",
"name": "GM17922 cell",
"definition": "[' NIEMANN-PICK DISEASE, TYPE C1; NPC1 NPC1 GENE; NPC1']",
"term_type": "cell line"
},
{
"accession": "CLO:0016276",
"name": "GM17923 cell",
"definition": "[' NIEMANN-PICK DISEASE, TYPE C1; NPC1 NPC1 GENE; NPC1']",
"term_type": "cell line"
},
{
"accession": "CLO:0016275",
"name": "GM17924 cell",
"definition": "[' NIEMANN-PICK DISEASE, TYPE C1; NPC1 NPC1 GENE; NPC1']",
"term_type": "cell line"
},
{
"accession": "CLO:0016274",
"name": "GM17926 cell",
"definition": "[' NPC1 GENE; NPC1 NIEMANN-PICK DISEASE, TYPE C1; NPC1']",
"term_type": "cell line"
},
{
"accession": "CLO:0016273",
"name": "GM17931 cell",
"definition": "[' XXY SYNDROME; KLINEFELTER SYNDROME ANEUPLOID CHROMOSOME NUMBER - NON-TRISOMIC']",
"term_type": "cell line"
},
{
"accession": "CLO:0016272",
"name": "GM17932 cell",
"definition": "[' CEREBELLAR HYPOPLASIA']",
"term_type": "cell line"
},
{
"accession": "CLO:0016271",
"name": "GM17918 cell",
"definition": "[' NPC1 GENE; NPC1 NIEMANN-PICK DISEASE, TYPE C1; NPC1']",
"term_type": "cell line"
},
{
"accession": "CLO:0016270",
"name": "GM17919 cell",
"definition": "[' NPC1 GENE; NPC1 NIEMANN-PICK DISEASE, TYPE C1; NPC1']",
"term_type": "cell line"
},
{
"accession": "CLO:0016269",
"name": "GM17920 cell",
"definition": "[' NPC1 GENE; NPC1 NIEMANN-PICK DISEASE, TYPE C1; NPC1']",
"term_type": "cell line"
}
]
}