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{
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"results": [
{
"accession": "CLO:0016972",
"name": "GM07335 cell",
"definition": "[' MAJOR AFFECTIVE DISORDER - 125480 OR 309200']",
"term_type": "cell line"
},
{
"accession": "CLO:0016973",
"name": "GM07336 cell",
"definition": "[' MAJOR AFFECTIVE DISORDER - 125480 OR 309200']",
"term_type": "cell line"
},
{
"accession": "CLO:0016974",
"name": "GM17594 cell",
"definition": "[' OSTEOGENESIS IMPERFECTA, TYPE IV; OI4 COLLAGEN, TYPE I, ALPHA-2; COL1A2']",
"term_type": "cell line"
},
{
"accession": "CLO:0016975",
"name": "GM17595 cell",
"definition": "[' OSTEOGENESIS IMPERFECTA, TYPE IV; OI4 COLLAGEN, TYPE I, ALPHA-2; COL1A2']",
"term_type": "cell line"
},
{
"accession": "CLO:0016976",
"name": "GM17596 cell",
"definition": "[' COLLAGEN, TYPE I, ALPHA-2; COL1A2 OSTEOGENESIS IMPERFECTA, TYPE IV; OI4']",
"term_type": "cell line"
},
{
"accession": "CLO:0016977",
"name": "GM17597 cell",
"definition": "[' COLLAGEN, TYPE I, ALPHA-2; COL1A2 OSTEOGENESIS IMPERFECTA, TYPE IV; OI4']",
"term_type": "cell line"
},
{
"accession": "CLO:0016978",
"name": "GM17598 cell",
"definition": "[' COLLAGEN, TYPE I, ALPHA-2; COL1A2 OSTEOGENESIS IMPERFECTA, TYPE IV; OI4']",
"term_type": "cell line"
},
{
"accession": "CLO:0016979",
"name": "GM17577 cell",
"definition": "[' COLLAGEN, TYPE I, ALPHA-2; COL1A2 OSTEOGENESIS IMPERFECTA, TYPE IV; OI4']",
"term_type": "cell line"
},
{
"accession": "CLO:0016980",
"name": "GM17576 cell",
"definition": "[' OSTEOGENESIS IMPERFECTA, TYPE IV; OI4 COLLAGEN, TYPE I, ALPHA-2; COL1A2']",
"term_type": "cell line"
},
{
"accession": "CLO:0016981",
"name": "GM17575 cell",
"definition": "[' CYSTINURIA; CSNU SOLUTE CARRIER FAMILY 3, MEMBER 1; SLC3A1']",
"term_type": "cell line"
},
{
"accession": "CLO:0016982",
"name": "GM17572 cell",
"definition": "[' XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP G; XPG']",
"term_type": "cell line"
},
{
"accession": "CLO:0016983",
"name": "GM17583 cell",
"definition": "[' RETT SYNDROME; RTT METHYL-CPG-BINDING PROTEIN 2; MECP2']",
"term_type": "cell line"
},
{
"accession": "CLO:0016984",
"name": "GM17586 cell",
"definition": "[' OSTEOGENESIS IMPERFECTA, TYPE IV; OI4 COLLAGEN, TYPE I, ALPHA-2; COL1A2']",
"term_type": "cell line"
},
{
"accession": "CLO:0016985",
"name": "GM17578 cell",
"definition": "[' COLLAGEN, TYPE I, ALPHA-2; COL1A2 OSTEOGENESIS IMPERFECTA, TYPE IV; OI4']",
"term_type": "cell line"
},
{
"accession": "CLO:0016986",
"name": "GM17579 cell",
"definition": "[' OSTEOGENESIS IMPERFECTA, TYPE IV; OI4 COLLAGEN, TYPE I, ALPHA-2; COL1A2']",
"term_type": "cell line"
},
{
"accession": "CLO:0016987",
"name": "GM17587 cell",
"definition": "[' OSTEOGENESIS IMPERFECTA, TYPE IV; OI4 COLLAGEN, TYPE I, ALPHA-2; COL1A2']",
"term_type": "cell line"
},
{
"accession": "CLO:0016988",
"name": "GM17588 cell",
"definition": "[' OSTEOGENESIS IMPERFECTA, TYPE IV; OI4 COLLAGEN, TYPE I, ALPHA-2; COL1A2']",
"term_type": "cell line"
},
{
"accession": "CLO:0016989",
"name": "GM17724 cell",
"definition": "[' FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1A; FSHMD1A (FSHD) FSHD GENE 1; FRG1']",
"term_type": "cell line"
},
{
"accession": "CLO:0016990",
"name": "GM17723 cell",
"definition": "[' SOLUTE CARRIER FAMILY 17, MEMBER 5; SLC17A5 SALLA DISEASE']",
"term_type": "cell line"
},
{
"accession": "CLO:0016991",
"name": "GM17729 cell",
"definition": "[' XXY SYNDROME; KLINEFELTER SYNDROME ANEUPLOID CHROMOSOME NUMBER - NON-TRISOMIC']",
"term_type": "cell line"
}
]
}