Terminology Service < Semantic Lookup Platform

All terms in NCIT

Label	Id	Description
Anti-CD2 Monoclonal Antibody	NCIT_C112882	[Any monoclonal antibody directed against the cell surface glycoprotein CD2, regardless of the antibody type.]
BRAF Gene Mutation	NCIT_C40430	[A change in the nucleotide sequence of the BRAF gene.]
RAF Family Gene Mutation	NCIT_C136425	[A change in the nucleotide sequence in a RAF family gene.]
BRAF Gene	NCIT_C18363	[This gene is involved in cell organization/biogenesis and the inhibition of apoptosis.]
BRAF Protein Variant	NCIT_C98307	[A variation in the amino acid sequence for the serine/threonine-protein kinase B-raf protein.]
Anti-CD3 Monoclonal Antibody	NCIT_C112883	[Any monoclonal antibody directed against the cell surface glycoprotein CD3, regardless of the antibody type.]
Proton Radiation	NCIT_C40431	[Radiation of protons during radioactive decay.]
Radiation, Charged Particles	NCIT_C18982	[A particle which carries a positive or negative electrical charge, typically an ionized atom or molecule, or an electron.]
Anti-CD4 Monoclonal Antibody	NCIT_C112884	[Any monoclonal antibody directed against the cell surface glycoprotein CD4, regardless of the antibody type.]
Neutron	NCIT_C40432	[An elementary particle with 0 charge and a mass about equal to that of a proton.]
Anti-CD5 Monoclonal Antibody	NCIT_C112885	[Any monoclonal antibody directed against the cell surface glycoprotein CD5, regardless of the antibody type.]
Juvenile Type Bilateral Ovarian Granulosa Cell Tumor	NCIT_C40434	[A granulosa cell tumor that involves both ovaries. It affects females in the first three decades of life.]
Potter Syndrome	NCIT_C40435	[A rare, lethal congenital malformation characterized by bilateral renal agenesis and the absence or decreased volume of amniotic fluid (oligohydramnios). The presence of oligohydramnios gives rise to congenital anomalies that include hypoplastic lungs, lower extremities abnormalities, and characteristic facial features (low-set ears, widely separated eyes, nose flattening, and receding chin). Newborn infants usually die of respiratory failure.]
IAPP wt Allele	NCIT_C112880	[Human IAPP wild-type allele is located in the vicinity of 12p12.1 and is approximately 25 kb in length. This allele, which encodes islet amyloid polypeptide protein, is involved in the modulation of insulin-stimulated glycogen formation.]
IAPP Gene	NCIT_C112879	[This gene plays a role in insulin-mediated glucose metabolism.]
12p12.1	NCIT_C13572	[A chromosome band present on 12p]
Ovarian Sex Cord-Stromal Tumor Associated with Peutz-Jeghers Syndrome	NCIT_C40436	[A sex cord-stromal tumor that arises from the ovary in a patient diagnosed with Peutz-Jeghers syndrome.]
Ovarian Sex Cord-Stromal Tumor of Mixed or Unclassified Cell Types	NCIT_C39978	[A sex cord-stromal tumor that arises from the ovary and lacks the morphologic features that belong to the categories of granulosa-stromal tumors, Sertoli-stromal tumors, or steroid cell tumors.]
Islet Amyloid Polypeptide	NCIT_C112881	[Islet amyloid polypeptide (89 aa, ~10 kDa) is encoded by the human IAPP gene. This protein plays a role in the regulation of glucose metabolism.]
Peptide Hormone	NCIT_C1746	[Small proteins that function as hormonal signals, synthesized and secreted by one tissue or organ with physiological effects on other tissues or organs.]