Terminology Service < Semantic Lookup Platform

All terms in NCIT

Label	Id	Description
Adult 18-65 Years Old	NCIT_C49685	[A person from 18 years to 65 years of age.]
Adult	NCIT_C17600	[A human who has reached reproductive age.]
Promonocyte to Lymphocyte Ratio Measurement	NCIT_C74652	[The determination of the ratio of promonocytes compared to all lymphocytes present in a sample. The measurement may be expressed as a ratio or percentage.]
EEFSEC wt Allele	NCIT_C126627	[Human EEFSEC wild-type allele is located in the vicinity of 3q21.3 and is approximately 273 kb in length. This allele, which encodes selenocysteine-specific elongation factor protein, is involved in the translation of selenocysteine-containing proteins.]
Phase IIa Trial	NCIT_C49686	[A clinical research protocol generally referred to as a pilot or feasibility trial that aims to prove the concept of the new intervention in question.]
Promyelocyte to Lymphocyte Ratio Measurement	NCIT_C74653	[The determination of the ratio of promyelocytes compared to all lymphocytes present in a sample. The measurement may be expressed as a ratio or percentage.]
Selenocysteine-Specific Elongation Factor	NCIT_C126628	[Selenocysteine-specific elongation factor (596 aa, ~65 kDa) is encoded by the human EEFSEC gene. This protein plays a role in the synthesis of selenocysteine-containing proteins.]
MYO1F wt Allele	NCIT_C126621	[Human MYO1F wild-type allele is located within 19p13.3-p13.2 and is approximately 57 kb in length. This allele, which encodes unconventional myosin-If, is involved in intracellular movement.]
MYO1F Gene	NCIT_C126620	[This gene plays a role in the movement of intracellular components.]
19p13.3-p13.2	NCIT_C13762	[A chromosome band present on 19p]
Body Frame Size	NCIT_C49680	[The categorization of a person's body frame into small, medium and large based on the measurement of wrist circumference or the breadth of the elbow.]
Unconventional Myosin-If	NCIT_C126622	[Unconventional myosin-If (1098 aa, ~125 kDa) is encoded by the human MYO1F gene. This protein plays a role in the transport of intracellular components.]
FRYL wt Allele	NCIT_C126624	[Human FRYL wild-type allele is located in the vicinity of 4p11 and is approximately 283 kb in length. This allele, which encodes protein furry homolog-like, plays a role in the modulation of both cell polarity and cell shape.]
Helmet Cell Count	NCIT_C74658	[The determination of the number of helmet cells present in a sample.]
Large Unstained Cell Count	NCIT_C74659	[The determination of the number of large unstained cells present in a sample.]
Tetanic Cataract	NCIT_C35068	[A cataract resulting from hypocalcemia.]
Cataract	NCIT_C26713	[Partial or complete opacity of the crystalline lens of one or both eyes that decreases visual acuity and eventually results in blindness. Some cataracts appear in infancy or in childhood, but most develop in older individuals. (Sternberg Diagnostic Surgical Pathology, 3rd ed.)]
Thalassemia	NCIT_C35069	[An inherited blood disorder characterized by a decreased synthesis of one of the polypeptide chains that form hemoglobin. Anemia results from this abnormal hemoglobin formation.]
Genetic Disorder	NCIT_C3101	[Genetic diseases are diseases in which inherited genes predispose to increased risk. The genetic disorders associated with cancer often result from an alteration or mutation in a single gene. The diseases range from rare dominant cancer family syndrome to familial tendencies in which low-penetrance genes may interact with other genes or environmental factors to induce cancer. Research may involve clinical, epidemiologic, and laboratory studies of persons, families, and populations at high risk of these disorders.]
Telangiectasia	NCIT_C28194	[Local dilatation of small vessels resulting in red discoloration of the skin or mucous membranes.]