Terminology Service < Semantic Lookup Platform

All terms in NCIT

Label	Id	Description
10p12.1	NCIT_C28753	[A chromosome band present on 10p]
Beta-3 Adrenergic Receptor	NCIT_C126973	[Beta-3 adrenergic receptor (408 aa, ~44 kDa) is encoded by the human ADRB3 gene. This protein plays a role in G protein-coupled receptor signaling, lipolysis, and thermogenesis.]
Sorted Cells	NCIT_C126974	[Cells separated and collected from a heterogeneous population based on physical, phenotypic, biochemical, and/or molecular properties, regardless of technique.]
Uterine Corpus Hydropic Leiomyoma	NCIT_C126975	[A variant of leiomyoma arising from the uterine corpus. It is characterized by conspicuous zonal edema. Hyalinization may also be present.]
Uterine Corpus Leiomyoma	NCIT_C3434	[A benign smooth muscle neoplasm arising from the body of the uterus. It is characterized by the presence of spindle cells with cigar-shaped nuclei, interlacing fascicles, and a whorled pattern.]
Piezoelectric Elastic Modulus Scanner	NCIT_C126976	[A device that maps the elasticity modulus of a material surface using a piezoresonance probe during scanning microscopy.]
Interleukin-15 Receptor Subunit Alpha	NCIT_C126970	[Interleukin-15 receptor subunit alpha (267 aa, ~28 kDa) is encoded by the human IL15RA gene. This protein is involved in interleukin-dependent signaling.]
Cytokine Receptor	NCIT_C17667	[A cytokine receptor is a protein on the cell surface that specifically binds cytokine ligands which are small proteins secreted by immune cells. These receptors mediate molecular functions such as signal transduction.]
ADRB3 Gene	NCIT_C126971	[This gene plays a role in the modulation of the physiological effects of catecholamines.]
ADRB3 wt Allele	NCIT_C126972	[Human ADRB3 wild-type allele is located in the vicinity of 8p11.23 and is approximately 4 kb in length. This allele, which encodes beta-3 adrenergic receptor protein, is involved in catecholamine-dependent G protein-coupled receptor signaling. Mutation and variation in the gene is associated with increased susceptibility to obesity.]
Salivary Secretion Pathway	NCIT_C91810
Calcium-Mediated Signaling Pathway	NCIT_C91460
8p11.23	NCIT_C13830	[A chromosome band present on 8p]
Human Parainfluenza Virus 4	NCIT_C112318	[The serotype labeled 4 of the viral species Human parainfluenza virus, which is a single-stranded, negative-sense RNA virus of the Paramyxoviridae family and Rubulavirus genus, and causes bronchiolitis and pneumonia in humans.]
Rubulavirus	NCIT_C14326	[A genus of Paramyxovirinae which includes Mumps Virus]
Human Parainfluenza Virus	NCIT_C125641	[A non-taxonomic group of paramyxoviruses that are cause of respiratory tract infections in humans. Infection is most common in infants and young children and symptoms may include fever, runny nose, and cough. Infection is usually self-limiting but can also cause more severe illness, such as croup or pneumonia.]
Hyaluronic Acid Measurement	NCIT_C112319	[The determination of the amount of hyaluronic acid present in a sample.]
Human Herpesvirus 5	NCIT_C112314	[A species of enveloped and spherical viruses with a capsid with T=16 icosahedral symmetry and surrounded by amorphous tegument, in the Herpesviridae family and Cytomegalovirus genus. The genome is composed of monopartite, linear double-stranded DNA. Human herpesvirus 5 is found in humans and causes mononucleosis-like symptoms in healthy individuals and pneumonia, hepatitis, encephalitis, myelitis, colitis, retinitis, neuropathy, mucoepidermoid carcinoma as well as other malignancies in immunocompromised persons, organ transplant recipients and newborn infants. Human herpesvirus 5 is transmitted congenitally or via direct person-to-person contact.]
Cytomegalovirus	NCIT_C14196	[A genus of the family herpesviridae, subfamily betaherpesvirinae, infecting the salivary glands, liver, spleen, lungs, eyes, and other organs, in which they produce characteristically enlarged cells with intranuclear inclusions.]
Human Herpesvirus 7	NCIT_C112315	[A species of enveloped and spherical viruses with a capsid with T=16 icosahedral symmetry and surrounded by amorphous tegument, in the Herpesviridae family and Roseolovirus genus. The genome is composed of monopartite, linear double-stranded DNA. Human herpesvirus 7 is found in humans and causes exanthema subitum in infants. Human herpesvirus 7 is transmitted via direct person-to-person contact.]