Terminology Service < Semantic Lookup Platform

All terms in NCIT

Label	Id	Description
CCL26 Gene	NCIT_C24780	[This gene plays a role in chemotaxis and intercellular signal transduction.]
CCL27 wt Allele	NCIT_C49744	[Human CCL27 wild-type allele is located within 9p13 and is approximately 4 kb in length. This allele, which encodes C-C motif chemokine 27 protein, is involved in the navigation of memory T lymphocytes to cutaneous sites in inflammatory processes.]
CCL27 Gene	NCIT_C24781	[This gene is involved in immunoregulation.]
CCL2 wt Allele	NCIT_C49745	[Human CCL2 wild-type allele is located within 17q11.2-q12 and is approximately 2 kb in length. This allele, which encodes C-C motif chemokine 2 protein, is involved in the mediation of immune cell chemotaxis during tissue injury.]
CCL2 Gene	NCIT_C20907	[This gene is involved in inflammatory processes and disease development.]
CCL23 wt Allele	NCIT_C49740	[Human CCL23 wild-type allele is located within 17q12 and is approximately 5 kb in length. This allele, which encodes C-C motif chemokine 23 protein, plays a regulatory role in the chemotactic activity of resting T-lymphocytes and monocytes, and neutrophils.]
CCL23 Gene	NCIT_C24777	[This gene is involved in pro-inflammatory processes.]
CCL24 wt Allele	NCIT_C49741	[Human CCL24 wild-type allele is located in the vicinity of 7q11.23 and is approximately 2 kb in length. This allele, which encodes C-C motif chemokine 24 protein, plays a role in the chemotactic activity of resting T lymphocytes and eosinophils, and neutrophils.]
CCL24 Gene	NCIT_C24778	[This gene is involved in the regulation of hematopoietic formation and inflammatory processes.]
Anterior Uveitis	NCIT_C35109	[Inflammation of the iris and anterior chamber of the eye.]
Fragile X Tremor/Ataxia Syndrome	NCIT_C126566	[An X-linked dominant inherited syndrome caused by mutations in the FMR1 gene. It is a late onset disorder, usually occurring after age 50. It affects males more frequently than females. It is characterized by abnormalities in the cerebellum and white matter. It manifests with intention tremor, ataxia, and cognitive disabilities. The symptoms worsen with age.]
Vasopressor	NCIT_C126567	[Any substance used in the treatment of hypotension. A vasopressor agent increases reduced blood pressure.]
Agent Affecting Cardiovascular System	NCIT_C78274	[An agent that exerts a physiologic effect on any anatomic entity that is part of the cardiovascular system, including the heart and blood vessels.]
GCNT3 Gene	NCIT_C126568	[This gene is involved in the glycosylation of mucins.]
Protein Glycosylation	NCIT_C16643	[The covalent chemical or post-translational biochemical addition of carbohydrate or glycosyl groups to peptides or proteins by glycosyl transferases.]
GCNT3 wt Allele	NCIT_C126569	[Human GCNT3 wild-type allele is located in the vicinity of 15q21.3 and is approximately 45 kb in length. This allele, which encodes beta-1,3-galactosyl-O-glycosyl-glycoprotein beta-1,6-N-acetylglucosaminyltransferase 3 protein, plays a role in mucin glycosylation.]
O-Glycan Biosynthesis Pathway	NCIT_C38841
Increased Uric Acid Level	NCIT_C35105	[A laboratory test result indicating abnormally high concentration of uric acid in the blood.]
Elevated Test Result	NCIT_C81326	[A result of a test that is higher than a previous value or a normal range of values.]
Spinocerebellar Ataxia Type 7	NCIT_C126562	[An autosomal dominant inherited neurodegenerative disorder caused by mutations in the ATXN7 gene. It is characterized by progressive cerebellar ataxia, including dysarthria and dysphagia, cone-rod and retinal dystrophy, and progressive central visual loss resulting in blindness.]