Terminology Service < Semantic Lookup Platform

All terms in NCIT

Label	Id	Description
11q Translocation	NCIT_C133693	[A cytogenetic abnormality that refers to any translocation involving the long arm of chromosome 11.]
Chromosome 10	NCIT_C13205	[The designation for each member of the tenth largest human autosomal chromosome pair. Chromosome 10 spans about 135 million base pairs and represents between 4 and 4.5% of the total DNA in normal diploid cells.]
Refractory Glioblastoma	NCIT_C146734	[A glioblastoma that is resistant to treatment.]
Refractory Malignant Glioma	NCIT_C142855	[Malignant glioma that does not respond to treatment.]
Gallbladder Necrosis, CTCAE 5.0	NCIT_C146735	[A disorder characterized by a necrotic process occurring in the gallbladder.]
Hepatic Necrosis, CTCAE 5.0	NCIT_C146736	[A disorder characterized by a necrotic process occurring in the hepatic parenchyma.]
Ataxia, CTCAE 5.0	NCIT_C146737	[A disorder characterized by lack of coordination of muscle movements resulting in the impairment or inability to perform voluntary activities.]
Hemorrhoids, CTCAE 5.0	NCIT_C146738	[A disorder characterized by the presence of dilated veins in the rectum and surrounding area.]
Back Pain, CTCAE 5.0	NCIT_C146739	[A disorder characterized by a sensation of marked discomfort in the back region.]
Aerosol Spray with Pump	NCIT_C68940	[A pump device that dispenses a precise aerosolized dose by actuation.]
CHD1 wt Allele	NCIT_C107120	[Human CHD1 wild-type allele is located within 5q15-q21 and is approximately 71 kb in length. This allele, which encodes chromodomain-helicase-DNA-binding protein 1, plays a role in the regulation of transcription by the modification of chromatin structure.]
CHD1 Gene	NCIT_C107119	[This gene is involved in the modification of chromatin structure.]
Chromodomain-Helicase-DNA-Binding Protein 1	NCIT_C107121	[Chromodomain-helicase-DNA-binding protein 1 (1710 aa, ~197 kDa) is encoded by the human CHD1 gene. This protein is involved in the regulation of transcription by the modification of chromatin structure.]
DAB2IP Gene	NCIT_C107122	[This gene may play a role in tumor suppression.]
Typhlitis, CTCAE 5.0	NCIT_C146730	[A disorder characterized by necrotizing enterocolitis in neutropenic patients.]
DAB2IP wt Allele	NCIT_C107123	[Human DAB2IP wild-type allele is located within 9q33.1-q33.3 and is approximately 218 kb in length. This allele, which encodes disabled homolog 2-interacting protein, may be involved in tumor suppression.]
Disabled Homolog 2-Interacting Protein	NCIT_C107124	[Disabled homolog 2-interacting protein (1189 aa, ~132 kDa) is encoded by the human DAB2IP gene. This protein may play a role in tumor suppression.]
Billion Colony Forming Units per Milliliter	NCIT_C68905	[A derived unit of viable cell concentration defined as the number of billion colony forming units (10E9 CFU) in one milliliter of substance.]
Distressed During the Past Week on a Scale of 0 to 10	NCIT_C107158	[A question about an individual's level of distress during the past week.]
Meter Squared per Second	NCIT_C68906	[A unit of diffusion coefficient in SI system.]