Terminology Service < Semantic Lookup Platform

All terms in NCIT

Label	Id	Description
Evaluated Activity Relationship Probability Code	NCIT_C93830	[A coded value specifying the likelihood of the identified cause of an adverse event.]
Retromolar Trigone	NCIT_C54223	[A triangular-shaped area of mucosa located posterior the last mandibular molar tooth.]
Evaluated Activity Relationship Uncertainty Code	NCIT_C93831	[A coded value specifying whether and to what degree this evaluation or observation has been asserted to be in doubt in any way.]
Lip and Oral Cavity	NCIT_C54224	[The lips are the structures that surround the mouth, which is the oral aperture that opens into the oral cavity. The oral cavity is the space bounded superiorly by the hard and soft palates, inferiorly by the tongue and laterally by the cheeks.]
Evaluated Result Relationship Probability	NCIT_C93832	[A number representing the likelihood of the identified cause of an adverse event.]
Limited Radiation Therapy	NCIT_C54225	[Cancer therapy using ionizing radiation to < 50% of the body.]
Evaluated Result Relationship Probability Code	NCIT_C93833	[A coded value specifying the likelihood of the identified cause of an adverse event.]
Thinking	NCIT_C54226	[Mental activity, not predominantly perceptual, by which one apprehends some aspect of an object or situation based on past learning and experience.]
Evaluated Result Relationship Uncertainty Code	NCIT_C93834	[A coded value specifying whether and to what degree this evaluation or observation has been asserted to be in doubt in any way.]
ATPase Gene	NCIT_C54227	[A class of genes that encode ATP hydrolyzing enzymes, which cycle between the ADP-bound inactive state and the ATP-bound active state. This cyclic activity generates energy for cellular consumption.]
Experimental Unit Identifier	NCIT_C93835	[A unique symbol that establishes identity of the experimental unit.]
Fanconi Anemia	NCIT_C62505	[An autosomal recessive genetic disorder characterized by bone marrow failure, skeletal abnormalities, and an increase incidence of development of neoplasias.]
Experimental Unit Status Date	NCIT_C93836	[The date (and time) on which the status is assigned to the experimental unit.]
FANCM wt Allele	NCIT_C54229	[Human FANCM wild-type allele is located in the vicinity of 14q21.3 and is approximately 65 kb in length. This allele, which encodes Fanconi anemia group M protein, is involved in a specific protein ubiquination that is necessary for DNA repair. Cytogenetic aberrations in the FANCM gene are both a cause of Fanconi anemia and a predisposing factor in the development of malignancies.]
Experimental Unit Subgroup Code	NCIT_C93837	[A coded value specifying the identification of uniform groups of subjects for separate analysis or treatment.]
Nifedipine	NCIT_C29290	[A dihydropyridine calcium channel blocking agent. Nifedipine inhibits the transmembrane influx of extracellular calcium ions into myocardial and vascular smooth muscle cells, causing dilatation of the main coronary and systemic arteries and decreasing myocardial contractility. This agent also inhibits the drug efflux pump P-glycoprotein which is overexpressed in some multi-drug resistant tumors and may improve the efficacy of some antineoplastic agents. (NCI04)]
Nisoldipine	NCIT_C29291	[A dihydropyridine calcium channel blocking agent. Nisoldipine inhibits the transmembrane influx of extracellular calcium ions into myocardial and vascular smooth muscle cells, causing dilatation of the main coronary and systemic arteries and decreasing myocardial contractility. This agent also inhibits the drug efflux pump P-glycoprotein which is overexpressed in some multi-drug resistant tumors and may improve the efficacy of some antineoplastic agents. (NCI04)]
Government Funding Mechanism Code	NCIT_C93838	[A coded value specifying the unique identifier for areas of extramural research activity applied to various funding mechanisms.]
Epoch Type Code	NCIT_C93828	[A coded value specifying the kind of epoch.]
T Acute Lymphoblastic Leukemia	NCIT_C3183	[Acute lymphoblastic leukemia of T-cell origin. It comprises about 15% of childhood cases and 25% of adult cases. It is more common in males than females. (WHO, 2001)]