Terminology Service < Semantic Lookup Platform

All terms in NCIT

Label	Id	Description
Lytic Metastatic Bone Lesion	NCIT_C35371	[A radiologic finding indicating the presence of bone destruction that results from the spread of cancer to the bone(s).]
Lytic Bone Lesion	NCIT_C41040
Rat Benign Endocardial Schwannoma	NCIT_C60336
Intraocular Lens Implant Device	NCIT_C49999	[A corrective lens that is designed to be implanted within the eye capsule to replace the natural lens.]
Lens Device	NCIT_C50030	[An electric or optical device designed to focus electromagnetic radiation.]
Rat Benign Ependymoma	NCIT_C60337
Rat Benign Fibrous Histiocytoma	NCIT_C60338
Rat Benign Granular Cell Tumor	NCIT_C60339
ATP7A Gene	NCIT_C74973	[This gene is involved in copper transport.]
Translocase Gene	NCIT_C158414	[Genes encoding a class of enzymes that catalyze the movement of ions or molecules across or within membranes.]
ATP Hydrolysis	NCIT_C19939	[ATP Hydrolysis is the cleavage of a high-energy phosphate bond of adenosine triphosphate by the addition of water. The energy derived from hydrolysis of ATP is used to drive metabolic reactions including nucleic acid and protein synthesis, to move molecules against concentration gradients (active transport), and to produce mechanical motion (contraction of microfibrils and microtubules).]
ATP7A wt Allele	NCIT_C74974	[Human ATP7A wild-type allele is located within Xq13.2-q13.3 and is approximately 139 kb in length. This allele, which encodes copper-transporting ATPase 1 protein, plays a role in the localization of copper ions. Mutations in the gene are associated with both Menkes disease and occipital horn syndrome.]
Copper-Transporting ATPase 1	NCIT_C74975	[Copper-transporting ATPase 1 (1500 aa, ~163 kDa) is encoded by the human ATP7A gene. This protein is involved in copper ion homeostasis.]
ATRX Gene	NCIT_C74976	[This gene plays a role in the regulation of both chromatin remodeling and transcription.]
Helicase Gene	NCIT_C26057	[Helicase Genes encode proteins that promote unwinding of 1.) RNA during splicing and translation or 2.) duplex DNA during replication or repair by binding cooperatively to single-stranded regions of DNA or to short regions of duplex DNA that are undergoing transient opening. (NCI)]
Homeobox Protein ARX	NCIT_C74970	[Homeobox protein ARX (562 aa, ~58 kDa) is encoded by the human ARX gene. This protein plays a role in transcription.]
ATRX wt Allele	NCIT_C74977	[Human ATRX wild-type allele is located within Xq13.1-q21.1 and is approximately 281 kb in length. This allele, which encodes transcriptional regulator ATRX protein, is involved in the modulation of both transcription and chromatin structure. Mutations in the gene are associated with X-linked alpha-thalassemia/mental retardation syndrome, mental retardation syndromic X-linked with hypotonic facies syndrome type 1, and alpha-thalassemia myelodysplasia syndrome.]
Neurotic Depression	NCIT_C35369	[A term used for any state of depression that is not psychotic.]
Depression	NCIT_C2982	[A melancholy feeling of sadness and despair.]
Transcriptional Regulator ATRX	NCIT_C74978	[Transcriptional regulator ATRX (2492 aa, ~283 kDa) is encoded by the human ATRX gene. This protein plays a role in both chromatin remodeling and transcriptional regulation.]