Terminology Service < Semantic Lookup Platform

All terms in NCIT

Label	Id	Description
Acute Undifferentiated Leukemia	NCIT_C9298	[A rare acute leukemia of ambiguous lineage in which the blasts do not express markers specific to myeloid or lymphoid lineage.]
Myocardial Disorder	NCIT_C35544	[A disorder that affects the muscle tissue of the heart. Representative examples include myocardial infarction, myocarditis, and cardiomyopathy.]
Nephrotic Syndrome with Lesion of Minimal Change Glomerulonephritis	NCIT_C35540	[A renal functional disorder characterized by proteinuria, edema, hyperlipidemia and hypoalbuminemia. It results from damage to the renal vascular filtration apparatus. It is further characterized by an inflammatory reaction in the glomerular capillaries and the effacement of the surrounding epithelial cell foot processes worsening protein leakage. Sequelae may include hypertension, atherosclerosis, infection, hypercoagulablity and renal failure.]
Polysomy 7	NCIT_C126119	[A numerical chromosomal abnormality characterized by the presence of more than two copies of chromosome 7 in a cell.]
Polysomy	NCIT_C36331	[The condition of having additional copies of a chromosome present in a cell.]
Chromosome 7 Abnormality	NCIT_C159455	[A cytogenic abnormality that refers to any structural irregularity in chromosome 7.]
Kinase Inhibitor Sensitivity	NCIT_C126115	[A metabolic marker that predicts which kinase inhibitor agent could be an effective treatment for a patient's tumor based on the in vitro treatment response for cells extracted from the tumor.]
Metabolic Marker	NCIT_C18520	[Specific metabolic changes that characterize an organism's state of health or disease, or response to a particular therapeutic intervention, and helps make diagnosis more accurate or enable physicians to make diagnosis before symptoms appear and to track disease progression.]
Nephrotic Syndrome with Lesion of Lobular Glomerulonephritis	NCIT_C35538
PGF Gene Product	NCIT_C126116	[A protein encoded by the PGF gene.]
PGF Gene	NCIT_C24670	[This gene plays a role in the growth, proliferation and migration of endothelial cells. It is also involved in angiogenesis.]
Nephrotic Syndrome with Lesion of Mesangiocapillary Glomerulonephritis	NCIT_C35539
Placenta Growth Factor Isoform 1	NCIT_C126117	[Placenta growth factor isoform 1 (149 aa, ~17 kDa) is encoded by the human PGF gene. This protein may be involved in the positive regulation of endothelial cell growth.]
HLA-Cw Serotype	NCIT_C126118	[A subset of serotypes for the HLA class I histocompatibility antigen, C alpha chain protein (HLA-C) found in the human population. Expression of Cw1 is associated with multinodular goiters, Cw6 is associated with susceptibility to psoriasis and alleles of Cw7 are associated with increased risk of age-related macular degeneration. Expression of Cw5 may be associated with increased risk of rheumatoid arthritis (RA) and expression of Cw4 may protect patients from RA, while Cw3 expression may be associated with increased risk of developing vascular complications for patients with RA. Expression of Cw4 may also be associated with reduced susceptibility to HIV-1 viremia.]
Molecular Signature	NCIT_C48181	[The set of characteristics, including the expression of certain genes, proteins, polysaccharides and/or lipids, that can identify what cells or tissues are present in a biological sample and/or indicate whether abnormal cells or tissues are present.]
Infant Acute Biphenotypic Leukemia	NCIT_C126111	[An acute biphenotypic leukemia that occurs in infancy.]
Acute Biphenotypic Leukemia	NCIT_C4673	[An acute leukemia of ambiguous lineage characterized by blasts which coexpress myeloid and T or B lineage antigens or concurrent B and T lineage antigens. (WHO, 2001)]
Nephrotic Syndrome with Lesion of Segmental Hyalinosis	NCIT_C35534	[A renal functional disorder characterized by proteinuria, edema, hyperlipidemia and hypoalbuminemia. It results from damage to the renal vascular filtration apparatus. It is further characterized by an inflammatory reaction in the filtering capillaries and the deposition of plasma components between the endothelium and glomerular basement membrane. Sequelae may include hypertension, atherosclerosis, infection, hypercoagulablity and renal failure.]
Infant T Acute Lymphoblastic Leukemia	NCIT_C126112	[A T acute lymphoblastic leukemia that occurs in infancy.]
Infant Acute Lymphoblastic Leukemia	NCIT_C122614	[An acute lymphoblastic leukemia that occurs in infancy.]