Terminology Service < Semantic Lookup Platform

All terms in NCIT

Label	Id	Description
7q22.1	NCIT_C13773	[A chromosome band present on 7q]
Histone-Lysine N-Methyltransferase 2E	NCIT_C93096	[Histone-lysine N-methyltransferase MLL5 (1858 aa, ~204 kDa) is encoded by the human MLL5 gene. This protein is involved in the methylation of histone proteins, the modulation of cell cycle progression and the regulation of gene transcription.]
RAD21 wt Allele	NCIT_C93086	[Human RAD21 wild-type allele is located in the vicinity of 8q24 and is approximately 29 kb in length. This allele, which encodes double-strand-break repair protein rad21 homolog, plays a role in the modulation of chromosome cohesion, the mediation of DNA repair and the regulation of apoptosis.]
RAD21 Gene	NCIT_C93082	[This gene is involved in chromosomal cohesion, DNA repair and apoptosis.]
Double-Strand-Break Repair Protein Rad21 Homolog	NCIT_C93087	[Double-strand-break repair protein rad21 homolog (631 aa, ~72 kDa) is encoded by the human RAD21 gene. This protein is involved in DNA repair, cell cycle-dependent chromosomal cohesion and apoptosis.]
Penile Implant	NCIT_C93088	[An implanted device that enables the penis to become erect.]
Implant	NCIT_C41075	[A prosthesis placed permanently in tissue.]
Fortified Food	NCIT_C93089
Pulmonologist	NCIT_C93080
Ethical Will	NCIT_C93081
Lassitude	NCIT_C93083	[Physical or mental fatigue.]
Prostration	NCIT_C93084
Self-esteem	NCIT_C93085
DDB2 Gene	NCIT_C93075	[This gene plays a role in DNA repair.]
Xeroderma Pigmentosum	NCIT_C3452	[An inherited skin disorder characterized by photosensitivity with severe sunburn in infancy, the development of numerous pigmented spots resembling freckles, larger atrophic lesions associated with telangiectasis, and multiple solar keratoses. Transmitted in an autosomal recessive manner, xeroderma pigmentosa involves a defect in nucleotide excision repair (NER), leading to deficient repair of DNA damaged by UV radiation and chromosome breakage. Individuals with this disease develop multiple malignant cutaneous neoplasms at an early age and may suffer from severe ophthalmic and neurologic abnormalities.]
DDB2 wt Allele	NCIT_C93076	[Human DDB2 wild-type allele is located within 11p12-p11 and is approximately 24 kb in length. This allele, which encodes DNA damage-binding protein 2, is involved in DNA repair. Mutation of the gene is associated with xeroderma pigmentosum complementation group E.]
DNA Damage-Binding Protein 2	NCIT_C93077	[DNA damage-binding protein 2 (427 aa, ~48 kDa) is encoded by the human DDB2 gene. This protein plays a role in the mediation of DNA repair.]
Podiatrist	NCIT_C93078
Urologic Oncologist	NCIT_C93079
Oncologist	NCIT_C17821	[A physician who specializes in the diagnosis and treatment of cancer.]