Terminology Service < Semantic Lookup Platform

All terms in EFO

Label	Id	Description
Gastric Small Cell Neuroendocrine Carcinoma	EFO_1000277	[An aggressive, high-grade and poorly differentiated carcinoma with neuroendocrine differentiation that arises from the stomach. It is characterized by the presence of malignant small cells.]
gastric neuroendocrine neoplasm	MONDO_0003111	[A neoplasm with neuroendocrine differentiation that arises from the stomach. It includes well differentiated neuroendocrine tumors (low and intermediate grade) and poorly differentiated neuroendocrine carcinomas (high grade).]
Stormorken syndrome	MONDO_0008497	[Stormorken-Sjaastad-Langslet syndrome is characterized by thrombocytopathy, asplenia, miosis, muscle fatigue, migraine, dyslexia, and ichthyosis. It has been described in six members of one family. It is transmitted as an autosomal dominant trait.]
Gastric Mucosa-Associated Lymphoid Tissue Lymphoma	EFO_1000274	[A low grade, indolent B-cell lymphoma, usually associated with Helicobacter pylori infection. Morphologically it is characterized by a dense mucosal atypical lymphocytic (centrocyte-like cell) infiltrate with often prominent lymphoepithelial lesions and plasmacytic differentiation. Approximately 40% of gastric MALT lymphomas carry the t(11;18)(q21;q21). Such cases are resistant to Helicobacter pylori therapy.]
Gastric Neuroendocrine Tumor G1	EFO_1000275	[A well differentiated, low grade neuroendocrine tumor (carcinoid tumor) that arises from the stomach. The vast majority of cases arise from the corpus-fundus region. The mitotic count is less than 2 per 10 HPF and/or the Ki67 index is equal to or less than 2 percent. It may be associated with autoimmune chronic atrophic gastritis, multiple endocrine neoplasia type 1, or it may be sporadic.]
gastric neuroendocrine tumor, well differentiated, low or intermediate grade	MONDO_0015062	[A well differentiated, low or intermediate grade tumor with neuroendocrine differentiation that arises from the stomach.]
1-O-oleoyl-sn-glycero-3-phosphocholine	CHEBI_28610	[An oleoyl-sn-glycero-3-phosphocholine in which the acyl group at position 1 is (9Z)-octadecenoyl (oleoyl) and the hydroxy group at position 2 is unsubstituted.]
Thalassiosira pseudonana	NCBITaxon_35128
1,4-dichlorobenzene	CHEBI_28618
obsolete_lymphoblastic leukemia MOLT-4	EFO_0000190
obsolete_MELAS syndrome	EFO_0000192	[A mitochondrial disorder characterized by focal or generalized seizures, episodes of transient or persistent neurologic dysfunction resembling strokes, and ragged-red fibers on muscle biopsy. Affected individuals tend to be normal at birth through early childhood, then experience growth failure, episodic vomiting, and recurrent cerebral insults resulting in visual loss and hemiparesis. The cortical lesions tend to occur in the parietal and occipital lobes and are not associated with vascular occlusion. VASCULAR HEADACHE is frequently associated and the disorder tends to be familial. (From Joynt, Clinical Neurology, 1992, Ch56, p117)]
obsolete_MMHCC part	EFO_0000193	[An MMHCC (Mouse Models of Human Cancers Consortium) part is an organism part that has been modelled by the MMHCC, a program to develop and refine experimental models that reflect the etiology and progression of human cancer., A program to develop and refine experimental models that reflect the etiology and progression of human cancer.]
acrylamide	CHEBI_28619	[A member of the acrylamides that has formula C3H5NO., This gene plays a regulatory role in the complement pathway, which is comprised of a complex proteolytic cascade.]
obsolete_malignant peripheral nerve sheath tumor class	EFO_0000194	[An uncommon, highly aggressive malignant tumor, arising from the peripheral nerves and affecting mostly adults in their third to sixth decades of life. It usually occurs in medium-sized and large nerves of the buttock, thigh, upper arm, or the paraspinal region. It may be associated with neurofibromatosis 1 (NF1)., Neoplasms which arise from nerve sheaths formed by SCHWANN CELLS in the PERIPHERAL NERVOUS SYSTEM or by OLIGODENDROCYTES in the CENTRAL NERVOUS SYSTEM. Malignant peripheral nerve sheath tumors, NEUROFIBROMA, and NEURILEMMOMA are relatively common tumors in this category.]
metabolic syndrome	EFO_0000195	[A cluster of metabolic risk factors for CARDIOVASCULAR DISEASES and TYPE 2 DIABETES MELLITUS. The major components of metabolic syndrome X include excess ABDOMINAL FAT; atherogenic DYSLIPIDEMIA; HYPERTENSION; HYPERGLYCEMIA; INSULIN RESISTANCE; a proinflammatory state; and a prothrombotic (THROMBOSIS) state. (from AHA/NHLBI/ADA Conference Proceedings, Circulation 2004; 109:551-556)]
metastatic prostate cancer	EFO_0000196	[A carcinoma that arises from the prostate gland and has spread to other anatomic sites.]
cytochalasin D	CHEBI_529996	[A mycotoxin, which is cell permeable and a potent inhibitor of actin polymerisation and DNA synthesis.]
mucin-producing carcinoma	MONDO_0020596
myelodysplastic syndrome	EFO_0000198	[A clonal hematopoietic disorder characterized by dysplasia and ineffective hematopoiesis in one or more of the hematopoietic cell lines. The dysplasia may be accompanied by an increase in myeloblasts, but the number is less than 20%, which, according to the WHO guidelines, is the requisite threshold for the diagnosis of acute myeloid leukemia. It may occur de novo or as a result of exposure to alkylating agents and/or radiotherapy. (WHO, 2001)]
myeloid hemopathy	MONDO_0015756