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{
"accession": "DOID:2477",
"name": "hereditary motor and sensory neuropathy",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "DOID:2741",
"name": "hereditary hyperbilirubinemia",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "DOID:1270",
"name": "hereditary hemorrhagic telangiectasia",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "DOID:1416",
"name": "hereditary eye disease",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "DOID:630",
"name": "hereditary disease",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "DOID:481",
"name": "hereditary degenerative disease of central nervous system",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "DOID:13269",
"name": "hereditary coproporphyria",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "DOID:9794",
"name": "Hereditary choroidal atrophy",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "DOID:3212",
"name": "hereditary central nervous system demyelinating disease",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "DOID:10585",
"name": "hereditary and idiopathic peripheral neuropathy",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "CLO:0003714",
"name": "HEPM cell",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "CLO:0037361",
"name": "HepG2-CYP2B6-hCAR",
"definition": "['HepG2 cells modified with a luciferase reporter responsive responsive to the activation of the contained constituitive androstane receptor and cytochrome 2B6']",
"term_type": "cell line"
},
{
"accession": "CLO:0003704",
"name": "Hep G2 cell",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "CLO:0037359",
"name": "HepG2-AhR-luc",
"definition": "['HepG2 cells modified with an aryl hydrocarbon receptor (AhR) luciferase reporter and 20 dioxin response elements']",
"term_type": "cell line"
},
{
"accession": "CLO:0003705",
"name": "HEP G2/2.2.1 cell",
"definition": "['disease: hepatocellular carcinoma; transfected with a CYP7 minigene/luciferase construct']",
"term_type": "cell line"
},
{
"accession": "UBERON:0004913",
"name": "hepatopancreatic ampulla",
"definition": "['A dilation of the duodenal papilla that is the opening of the juncture of the common bile duct and the main pancreatic duct.']",
"term_type": "cell line"
},
{
"accession": "DOID:893",
"name": "hepatolenticular degeneration",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "DOID:5230",
"name": "hepatoerythropoietic porphyria",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "CL:0000182",
"name": "hepatocyte",
"definition": "['The main structural component of the liver. They are specialized epithelial cells that are organized into interconnected plates called lobules. Majority of cell population of liver, polygonal in shape, arranged in plates or trabeculae between sinusoids; may have single nucleus or binucleated.', 'Hepatocytes are reportedly MHC Class I-positive and MHC Class II-positive.']",
"term_type": "cell line"
},
{
"accession": "DOID:684",
"name": "hepatocellular carcinoma",
"definition": "['A liver carcinoma that has_material_basis_in undifferentiated hepatocytes and located_in the liver.', 'OMIM mapping confirmed by DO. [SN].']",
"term_type": "cell line"
}
]
}