Terminology Service < Semantic Lookup Platform

All terms in NCIT

Label	Id	Description
Necrobiosis Lipoidica	NCIT_C34840	[An uncommon inflammatory skin condition, often associated with diabetes mellitus, that is characterized by the formation of multiple shiny atrophic lesions thought to be due to collagen degeneration with a granulomatous response, thickening of blood vessel walls, and fat deposition. The lesions are usually found on the leg.]
Necatoriasis	NCIT_C34838	[A disorder caused by an infection with hookworms of the genus Necator, which settle in the host's small intestine, and cause abdominal pain, diarrhea, weight loss, and anemia.]
Neck Sprain	NCIT_C34839	[Stretching or tearing of ligaments in the neck.]
Myxedema	NCIT_C34834	[A condition characterized by severe hypothyroidism that is caused by autoimmune thyroid gland disorders, surgical reduction of thyroid tissue, radiation exposure, and viral infections. Signs and symptoms include generalized fatigue, lethargy, increased body weight, pale, edematous and thickened skin, low blood pressure, constipation and cold intolerance.]
Nabothian Cyst	NCIT_C34835	[A benign, mucus-filled cervical cyst that occurs when mucus-secreting columnar epithelial cells are covered with squamous epithelium.]
Uterine Cervix Cyst	NCIT_C3977	[A cyst in the uterine cervix.]
Ingrown Toenail	NCIT_C34836	[A condition in which the nail grows into the nailbed secondary to downward pressure, generally caused by ill-fitting shoes. Symptoms include pain, erythema, and edema, and may result in infection if it remains untreated.]
Nasopharyngitis	NCIT_C34837	[An inflammatory process that affects the nasopharynx.]
Pharyngitis	NCIT_C26851	[Inflammation of the throat most often caused by viral and bacterial infections. Other causes include allergens, chemical substances, and trauma.]
Cardiomyopathy	NCIT_C34830	[A disease of the heart muscle or myocardium proper. Cardiomyopathies may be classified as either primary or secondary, on the basis of etiology, or on the pathophysiology of the lesion: hypertrophic, dilated, or restrictive.]
Myoclonic Jerk	NCIT_C34832	[A sudden, involuntary contraction of a muscle or group of muscles; these movements may develop as a symptom of a number of neurological diseases, including epilepsy, Parkinson's disease, Alzheimer's disease, or Creutzfeldt-Jacob disease.]
Motor Manifestations	NCIT_C5039	[The presence of an alteration in the ability to move one's body or any body parts in accordance with one's intent.]
Myotonic Cataract	NCIT_C34833	[A cataract occurring as a sequela of myotonic dystrophy.]
Myotonic Dystrophy	NCIT_C84914	[An inherited progressive disorder affecting the muscles. It is characterized by muscle wasting and hypotonia, cataracts, heart conduction defects and endocrinopathies.]
Night Blindness	NCIT_C34850	[Inability to see clearly in dim light.]
Blindness	NCIT_C97109	[The lack of vision. It is caused by neurological or physiological factors.]
Visual Manifestations	NCIT_C5042
Increased NPN	NCIT_C34851	[A laboratory test result indicating abnormally high concentration of non-protein nitrogen in the blood.]
TEP1 Gene	NCIT_C20208	[This gene plays a role in telomerase activity.]
Epithelial Cell Adhesion Molecule	NCIT_C20209	[Epithelial cell adhesion molecule (314 aa, ~35 kDa) is encoded by the human EPCAM gene. This protein is involved in both cell adhesion and cellular proliferation.]