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{
"accession": "DOID:0002116",
"name": "pterygium",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "DOID:0050117",
"name": "disease by infectious agent",
"definition": "['\"A disease that is the consequence of the presence of pathogenic microbial agents, including pathogenic viruses, pathogenic bacteria, fungi, protozoa, multicellular parasites, and aberrant proteins known as prions.\" [DO:wk]']",
"term_type": "cell line"
},
{
"accession": "DOID:0050120",
"name": "hemophagocytic syndrome",
"definition": "['\"A syndrome that is characterized by an expansion of the monocyte-macrophage population and intense hemophagocytosis. It can occur de novo, but more often occurs in the setting of another disorder, usually an infection or a malignancy. A clinical picture of fever, hepatosplenomegaly, lymphadenopathy and peripheral pancytopenia. The morphologic hallmark of this syndrome is the phagocytosis of hematopoietic elements by morphologically normal macrophages.\" [url:http\\\\://www.mayoclinicproceedings.com/inside.asp?AID=57&UID=, url:http\\\\://www.scielo.br/scielo.php?script=sci_arttext&pid=S1516-31801997000500007&lng=pt&nrm=iso]']",
"term_type": "cell line"
},
{
"accession": "DOID:0050144",
"name": "Kartagener syndrome",
"definition": "['\"A syndrome consisting of triad of sinusitis, bronchiectasis and situs inversus with dextrocardia.\" [url:http\\\\://www.ncbi.nlm.nih.gov/pubmed/19529061]']",
"term_type": "cell line"
},
{
"accession": "DOID:0050155",
"name": "sensory system disease",
"definition": "['\"A body system disease which is located in a part of the nervous system responsible for processing sensory information that consists of sensory receptors, neural pathways, and parts of the brain involved in sensory perception. Commonly recognized sensory systems are those for vision, hearing, somatic sensation (touch), taste and olfaction (smell).\" [url:http\\\\://en.wikipedia.org/wiki/Sensory_system]']",
"term_type": "cell line"
},
{
"accession": "DOID:0050161",
"name": "lower respiratory tract disease",
"definition": "['\"A respiratory system disease which involves the lower respiratory tract.\" [url:http\\\\://en.wikipedia.org/wiki/lower_respiratory_tract]']",
"term_type": "cell line"
},
{
"accession": "DOID:0050177",
"name": "simple genetic disease",
"definition": "['\"A hereditary disease that is the result of one or more abnormal alleles and may be dominant (a single copy of the abnormal allele is sufficient to give rise to the disease), semi-dominant, or recessive (requiring both copies of the gene to have an abnormal allele).\" [DO:wk\\\\,ls]']",
"term_type": "cell line"
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{
"accession": "DOID:0050324",
"name": "physical disorder",
"definition": "['\"A disorder that has an available objective mechanical test (such as chemical tests or brain scans), and are diagnosed only by behavioral syndrome (such as those in the Diagnostic and Statistical Manual of Mental Disorders (DSM).\" [url:http\\\\://en.wikipedia.org/wiki/Physical_disorder]']",
"term_type": "cell line"
},
{
"accession": "DOID:0050325",
"name": "genetic disorder",
"definition": "['\"A disorder that is caused by abnormalities in an individual\\'s genetic material (genome).\" [url:http\\\\://www.ornl.gov/sci/techresources/Human_Genome/medicine/assist.shtml]']",
"term_type": "cell line"
},
{
"accession": "DOID:0050328",
"name": "functional disorder",
"definition": "['\"A disorder that impairs the normal function of a bodily process.\" [url:http\\\\://en.wikipedia.org/wiki/Functional_disorder]']",
"term_type": "cell line"
},
{
"accession": "DOID:0050424",
"name": "familial adenomatous polyposis",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "DOID:0050425",
"name": "restless legs syndrome",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "DOID:0050427",
"name": "xeroderma pigmentosum",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "DOID:0050436",
"name": "Mulibrey nanism",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "DOID:0050439",
"name": "Usher syndrome",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "DOID:0050441",
"name": "multiple sulfatase deficiency disease",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "DOID:0050442",
"name": "Niemann-Pick disease type A",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "DOID:0050443",
"name": "Niemann-Pick disease type B",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "DOID:0050444",
"name": "infantile refsum disease",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "DOID:0050445",
"name": "hypophosphatemic rickets X-linked dominant",
"definition": "[]",
"term_type": "cell line"
}
]
}